Used Sterilization for sale (207)

Year of construction: 2002, condition: used, This listing is for the Ehret STE 1610/2/100 Sterilising Oven. The unit is in full working condition and is ready for immediate use. Overview The Ehret STE 1610/2/100 Sterilising Oven is a high-performance dry heat sterilizer designed for reliable and consistent sterilization of laboratory and pharmaceutical materials. Manufactured by Ehret, a trusted German brand in thermal processing equipment, the STE 1610/2/100 delivers precise temperature control and robust performance, making it ideal for applications requiring sterilization without moisture, such as glassware, metal instruments, and heat-stable laboratory components. Key Features Precise Dry Heat Sterilization Fpodpfx Aaoxhflxo Eed High-Temperature Range: Operates up to 250 °C, suitable for complete sterilization and thermal decontamination. Uniform Temperature Distribution: Advanced air circulation ensures even heat distribution throughout the chamber. Validated Sterilization Cycles: Ideal for sterilizing glass, metal tools, and other heat-resistant materials with accuracy and repeatability. Robust Construction & Ergonomic Design Durable Stainless Steel Chamber: Corrosion-resistant and easy to clean, suitable for repeated sterilization cycles. User-Friendly Controls: Digital temperature controller with display for accurate setpoint adjustment and monitoring. Safety Features: Over-temperature protection, door interlock, and visual/audio alarms for enhanced operational safety. Technical Specifications Model: STE 1610/2/100 Temperature Range: Ambient +5 °C to 250 °C Chamber Volume: Approx. 100 litres Heating Method: Electrically heated with forced air circulation Temperature Control Accuracy: ±1 °C Construction: Stainless steel inner chamber; powder-coated steel exterior Control System: Digital PID controller with safety cut-off and time functions Power Supply: 230 V / 50–60 Hz (depending on configuration) Applications Pharmaceutical Laboratories: Dry sterilization of vials, stoppers, and instruments Medical Facilities: Sterilizing surgical tools, metal parts, and reusable components Research & Diagnostics: Sterilization of labware and experimental setups Industrial & QA Labs: Heat treatment, drying, and thermal conditioning of materials System Components Electrically heated drying/sterilization chamber Forced air circulation fan for uniform heating Digital control panel with setpoint and actual temperature display Safety thermostat with alarm system Removable shelving for flexible loading Quality Assurance All Ehret STE ovens are manufactured in compliance with DIN and ISO standards and undergo rigorous quality testing at the factory. Designed for reliable long-term use, the units support calibration, validation (IQ/OQ), and GMP documentation where required. Benefits Reliable Sterilization: Proven performance across thousands of cycles Accurate & Uniform Heating: Ensures consistent results and safe sterilization Low Maintenance: Durable components and easy-to-clean surfaces Safety-Compliant: Built with laboratory and industrial safety standards in mind Compact Footprint: Fits easily into lab or cleanroom environments Conclusion The Ehret STE 1610/2/100 Sterilising Oven is a dependable, precision-controlled dry heat sterilizer built for modern lab and pharmaceutical environments. Its combination of German engineering, validated performance, and operator-friendly design makes it a trusted solution for high-integrity sterilization processes.

Condition: used, Combi filter (kieselgur- and sterilising filter) for beer filtration with hydraulic pressure, 100 x 100 cm filter plates and external risers. Additional title: combination filter Fpsdpfovcqlwex Aa Eod Capacity: 120 hl/h Plate size: 100 cm edge length Length: 7000 mm Width: 1500 mm Height: 1500 mm Position: horizontal Base construction: mounted on steel frame, standing on feet Features: 31 kieselguhr layers (32 frames), 50 sterilisation layers, 4 pressure manometers (10bar), 6 lanterns, risers, kieselguhr discharge screw (Allweiler), gravity measurement, flow measurement, 3 x turbidity measurement (inlet, outlet Kieselgur filter, outlet 3 x turbidity measurement (inlet, outlet kieselgur filter, outlet sterilisation filter). Spare parts: 295 sealing rings for filter plates, 3 kieselguhr filter support plates

Condition: good (used), Good working condition. Please check out our other listings as well. Fodpfxoqmiwao Aa Ejpd

Condition: excellent (used), functionality: fully functional, The Olimpic TC sterilization plant stands out for its high performance and maximum reliability, specifically designed to process products with higher consistency and viscosity. Products: Ketchup, Sauces, Jams, Tomato, etc. Viscosity: High viscosity. The Rossi & Catelli Olympic multi-tube aseptic sterilizer is a continuous heat exchange system designed for the sterilization of liquid and semi-liquid food products, such as juices, concentrates, purees, sauces, and products with small particles in suspension. It uses a system of concentric or parallel tubes to rapidly heat the product to high temperatures (HTST/UHT), followed by controlled cooling, guaranteeing the preservation of its organoleptic and nutritional properties. INCLUDED: * 13 temperature holding tubes, total: 65 tubes Fpedpswn Hbkjfx Aa Ejd * Cleaning cip with 1 citric acid tank and 1 ascorbic acid tank with agitator: 1.15 m diameter x 1.90 m high * Double dosing pump: 0.80 m x 0.50 m x 0.90 m. * SPIRAX ARC tubular heat exchanger * Hot water recirculation pump * Set of valves: 1.90 m x 1 m x 1.90 m * 2 Flow meters with electrical panel: 1 m x 0.77 m x 2 m The production may vary depending on the product.

Condition: used, Used Alfa Laval model BTPX 205SGD-34CDP-50 stainless steel clarifier centrifuge. Skid mounted system with steam sterilization provision. Direct driven by 6.5 kW 415V 3/50 2900 rpm motor. Maximum bowl speed 9650 rpm. Includes some tools. Fodpfeyh I Uuex Aa Eopd

Condition: good (used), MMM Group Vakulab HL Medical Autoclave Fpedjyifqvjpfx Aa Eod This listing is for the MMM Group Vakulab HL Medical Autoclave. The unit is in full working condition and is ready for immediate use. Overview The Vakulab HL autoclave from MM Group Medical is a high-performance, GMP-compliant sterilizer designed for the safe, reliable, and validated sterilization of laboratory instruments, equipment, and materials. Specifically engineered for use in pharmaceutical manufacturing, biotechnology facilities, and research laboratories, the Vakulab HL combines advanced vacuum-assisted steam sterilization with robust stainless steel construction to ensure consistent results in even the most demanding applications. Key Features inc Advanced Steam Sterilization, Pre- and Post-Vacuum Cycles: Ensures efficient steam penetration and rapid drying, Optimized Steam Distribution: Uniform sterilization across all load types Programmable Cycles: Fully adjustable parameters for different sterilization needs. GMP & Cleanroom Ready, Double-Door Pass-Through Design (optional): For installation between clean and non-clean areas, Stainless Steel Chamber & Piping: High-grade AISI 316L for corrosion resistance and hygienic operation, Integrated Monitoring: Real-time cycle control with full batch documentation capability. Operational Safety & Control User-Friendly HMI: Touchscreen interface for programming and monitoring, Automatic Door Operation: With safety interlocks to prevent accidental opening under pressure, Built-In Diagnostics: Self-check functions for preventive maintenance. Technical Specifications. The Vakulab HL is a vacuum-assisted steam sterilizer available in multiple chamber volumes, typically ranging from 300 to 1,000 liters. The sterilization process operates at temperatures between 121 °C and 134 °C, controlled via a PLC-based system with an intuitive touchscreen human-machine interface (HMI). steam, water, compressed air, and electricity. It is designed to meet EN 285, PED, ISO 9001, and GMP compliance requirements, and can be validated to ISO 17665 sterilization standards. Applications - Pharmaceutical Manufacturing: Sterilization of equipment, components, and containers, Biotechnology: Sterilization of fermentation vessels, culture media, and instruments, Research Laboratories: Sterilization of glassware, tools, and lab consumables, Hospitals & Clinical Settings: Safe sterilization of surgical instruments and textiles, System Components, High-grade stainless steel chamber with polished finish, Vacuum pump system for pre- and post-cycle air removal, Steam generation and distribution system, Control panel with PLC and HMI touchscreen, Integrated temperature and pressure sensors for validation. Quality & Compliance, Manufactured in accordance with GMP guidelines, Complies with EN 285 and ISO 17665 sterilization standards, Full FAT/SAT/IQ/OQ/PQ support for validation in regulated environments, Designed for integration into cleanroom and production facilities, Benefits - Consistent, Validated Sterilization for a wide range of load types.

Year of construction: 2018, condition: used, This listing is for a Solaris Biotech Solution Jupiter 3.0 Fermentor. The unit is in full working condition and is ready for immediate release. The Solaris Biotech Solution Jupiter 3.0 Fermentor is a highly versatile and configurable bioreactor system, ideal for laboratory-scale applications. With advanced automation and robust design, it caters to a wide range of research and development needs, as well as small-scale production. Key Features: Autoclavable and Sterilizable Design: Ensures ease of cleaning, sterility, and reliable operation for contamination-free processes. Flexible Vessel Options: Available in various aspect ratios and thermoregulation designs, with total volumes ranging from 2.0 L to 10.0 L. Pressure Control: Handles pressures up to 1.6 bar in the 2 L and 4 L jacketed vessels, with continuous gas-in and gas-out flux. Innovative SCADA Software (LEONARDO 3.0): Provides automated management of fermentation and cultivation processes, ensuring precision and ease of operation. Parallel Management: Supports simultaneous operation of up to 24 units via a single HMI with a 24” display, streamlining complex workflows. Remote Access: Enables monitoring and control via PC, tablet, or smartphone, using QR code scanning or a dedicated web portal for remote convenience. Applications: Process Development and Optimization: Facilitates experimentation and optimization of bioprocesses for scale-up and scale-down studies. Education and Research: Suitable for educational purposes and basic research in bioprocessing. Small-Scale Production: Supports small-batch manufacturing and pilot-scale processes. Benefits: Cost-Effective Performance: Combines advanced features with affordability for laboratory and production environments. High Level of Automation: Simplifies management of fermentation and cultivation with LEONARDO 3.0 software, reducing operator workload. Versatility and Configurability: Fsdpexxz T Hjfx Aa Eepd Adaptable to a wide variety of applications, ensuring compliance with validated GMP regulations. Technical Specifications: Material: VALOX resin (external) and silicone (internal) Autoclavable: 121-133°C for up to 30 minutes Residual Volume: 0.04 mL Flow Rate: 65 mL/min

Condition: good (used), Pharmatec 500-S4 Multistage pressure column distillation unit Fjdpfxoyfhtno Aa Ejpd Stainless, designed for the production of sterile, non-pyrogenic water for injection (WFI), all mounted on skid, four column system, 660 l/h pressurized heating steam, 4Bar, adjustable controls, 3Ph

Condition: excellent (used), Year of construction: 2018, Brinox SVMHI-550 Sterile Hold Vessel 550L 316L Stainless Steel Fjdpfx Aeymymvsa Ejpd Year 2018 Test Pressure 7.2 Bar Very little use. Tanks are in excellent condition.

Year of construction: 2002, condition: used, This listing is for a Lancer Washer Infeed Type 1600 PCM DPSS The unit is in full working condition and is ready for immediate release. Lancer 1600 PCM Stainless Steel Washer Overview The Lancer Washer Infeed Type 1600 PCM DPSS is a superior pharmaceutical production washer designed to exceed all GMP requirements Ehret Technologies – Trio-Tech International. This industrial-grade washing system is specifically engineered for pharmaceutical and laboratory applications where stringent cleaning standards are essential. Key Features Designed to provide an adequate cleaning process using mechanical, thermal and chemical cleaning properties ETO Sterilizer - Fully Automatic ETO Sterilizer, Hospital Sterilizer Manufacturer Multi-level washing capabilities for maximum efficiency GMP (Good Manufacturing Practice) compliant design Pharmaceutical-grade construction and validation Chamber Specifications Internal chamber dimensions: 33 5/8"H × 27 3/4"D × 27 3/4"W ETO Sterilizer - Fully Automatic ETO Sterilizer, Hospital Sterilizer Manufacturer Large capacity design for high-volume processing Multiple rack positions for flexibility Construction & Materials 316L Stainless Steel Construction: Pharmaceutical-grade stainless steel throughout for corrosion resistance and easy sanitization cGMP Compliant: Meets current Good Manufacturing Practice requirements Robust Design: Built for continuous industrial use in demanding environments Control System Microprocessor-controlled operation Multiple programmable wash cycles Process monitoring and documentation capabilities Applications Pharmaceutical manufacturing equipment cleaning Laboratory glassware and instrument washing Medical device processing Research facility applications Fodpfx Aajxhfkuo Ejpd Biotechnology equipment cleaning Technical Specifications Model: 1600 PCM (Pharmaceutical Cleaning Module) Construction: 316L Stainless Steel Compliance: cGMP, FDA regulations Operation: Automated wash/rinse/dry cycles Chemical Integration: Automated detergent and rinse aid dosing Validation: IQ/OQ/PQ documentation available Benefits Ensures consistent, validated cleaning results Reduces manual labour and contamination risk Meets strict pharmaceutical industry standards Large capacity increases throughput Automated operation improves efficiency and traceability This washer represents Lancer's commitment to providing pharmaceutical-grade cleaning solutions that meet the most demanding industry requirements for cleanliness, validation, and regulatory compliance.

Condition: used, Year of construction: 2008, operating hours: 34,590 h, machine/vehicle number: R81, Used Aseptic Filling Machine Tetra Pak A3/Flex 150V TBA 1000B – Overview This second hand Tetra Pak A3/Flex 150V TBA 1000B is a proven aseptic carton filler engineered for industrial packaging and beverage production. Configured for Tetra Brik Aseptic 1000 ml (Base) packs, it delivers reliable, continuous operation for UHT milk, juices, and other shelf-stable beverages. With a nominal capacity of approximately 7,000 packs/hour, this used bottling line component combines high throughput with aseptic integrity for modern carton packaging. Technical Specifications & Performance Data Fodpfxox H Thue Aa Eopd Manufacturer: Tetra Pak Model: A3/Flex 150V TBA 1000B Year of manufacture: 2008 Filling type: Aseptic (non-isobaric carton filling) Package format: Tetra Brik Aseptic 1000 ml (Base) Nominal speed: ≈ 7,000 packs/hour Working hours: ≈ 30,000 hours Utilities Electrical: 400 V, 50 Hz, 3-phase Installed power: up to ≈ 50 kW (typ. 35–50 kW depending on configuration) Compressed air: 6–8 bar, ≈ 300–500 Nl/min Water/steam: ≈ 0.5–1.0 m³/h (for processing/sterilization utilities) Dimensions & Weight Approximate footprint (L × W × H): 7 × 3 × 4.5 m Approximate weight: ≈ 7,000 kg (model range 6,000–8,000 kg) Note: Technical values are indicative for this A3/Flex configuration and should be confirmed during inspection/FAT. Advanced Automation & Control Systems The A3/Flex platform features OEM PLC-based control with a touchscreen HMI for recipe handling, alarms, and diagnostics. Motion control synchronizes forming, filling, and sealing cycles to maintain aseptic integrity and packaging quality at high speeds. Typical capabilities include: Recipe management for UHT milk, juices, and beverage variants Integrated process supervision and event/alarm logs I/O provisions for upstream/downstream line devices Recommended verification prior to start-up: PLC functions, valve actuation, pump performance, and seal integrity Production Line Integration Capabilities This aseptic carton filler integrates efficiently within a used bottling line or new beverage production layout: Upstream: packaging material feed and sterilization modules as per OEM design Downstream: conveyors to accumulation, straw/cap applicators, case packers, palletizers Utilities/process: interfaces for CIP/SIP connection to plant systems, sterile air, water, and steam Controls: standard digital/analog I/O and fieldbus-ready architecture depending on configuration Ideal for second hand industrial packaging projects requiring aseptic carton formats and stable high-speed operation. Machine Condition & Maintenance History Condition: used, currently in storage Approximate machine hours: ≈ 30,000 Operational note: continuous production achievable with proper preventive maintenance Recommended checks before commissioning: pumps, aseptic valves, PLC functionality, elastomers and seals Routine inspection, replacement of wear parts, and validation of aseptic barriers are advised prior to restart. Operational Performance & Versatility Product scope: UHT milk, juice, and shelf-stable beverages

Year of construction: 2014, condition: good (used), Mechatronics RPU-2100R Reagent Production Unit The Mechatronics RPU-2100R is a reagent production unit used in hematology to optimize reagent logistics in laboratories. The unit is manufactured by RR Mechatronics and is often used in combination with hematology analyzers from Sysmex. Purpose and Function The RPU-2100R (Reagent Production Unit) is used to automatically dilute concentrated reagents (such as Cellpack S Conc.) and produce large quantities of ready-to-use reagent on-site in the laboratory. The RPU-2100R is a standalone unit with all components housed in a single, enclosed enclosure. The enclosure features removable, epoxy-coated metal covers. All external connections and the ON/OFF switch are located on the rear of the unit. All user-serviceable and replaceable components are accessible via the front door. The cart for the Cellpack concentrate (e.g., Cellpack®-S Conc.) can be attached to any three sides of the unit. Features and Capacities The RPU-2100R focuses on optimizing reagent management for high-throughput laboratories: Reagent Concentrates: Uses Cellpack S Conc. in 10L and 20L containers. Throughput per Concentrate: Up to 8,250 complete blood counts per month can be performed with a 10L container without reagent changes. Up to 16,500 complete blood counts per month are possible with a 20L container. Shelf Life: Once opened, the reconstituted reagent has a shelf life of 30 days. Manufacturer: RR Mechatronics Model: RPU-2100R Catalog Number: NARP109010 External Connections Power Supply, Euro Plug Ethernet/USB (NARP109010 only) RJ45/USB-B RS-232 (NARP109000 only) 9-Pin SUB D Connector External Connections (Liquids) Fsdpfeyk U Dwsx Aa Eepd Water Connection: G ¾" Thread Reagent Dispensing Connections (4x) Push-in Hose Connection, 6 mm Outer Diameter Waste Connection (1x) Hose Barb, 12 mm Inner Diameter Reagent Concentrate Maximum Dimensions: 390 x 260 x 300 mm (W x D x H) Reagent: SYSMEX Cellpack Concentrate Peak Reagent Dispensing Rate: 0.5 Liters/Minute for 6 Minutes max. (at (with full reservoir and overflow tank and new pre-filter) 1 liter/minute, 2 minutes max. Filtration: Air filter, bacteria filter, pore size 0.2 µm Liquid pre-filter: Particle filter (sterilized), pore size 0.8+0.45 µm, self-venting Liquid final filter: Bacteria filter (sterilized), pore size 0.2 µm, self-venting System dimensions: Width: 500 mm Height: 700 mm Depth: 430 mm Weight: approx. 50 kg Water tank volume: 2.5 liters Reservoir: 2.5 liters Mixing tank: 0.6 liters Overflow tank: 0.6 liters Language selection available: German, English, Spanish, French, Hungarian, Italian, Dutch, Swedish Swedish (spreadable) Voltage: 230 VAC (+/- 10%) Frequency: 50-60 Hz Year of manufacture: 2014 Find more items – new and used – in our shop! International shipping costs available upon request!

Condition: used, This listing is for the Palltronic Flowstar 1V The unit is in full working condition and is ready for immediate use Palltronic Flowstar IV Filter Integrity Testing Instrument (and variants like Pall FFS04 S Palltronic Flowstar IV Filter Integrity Test Instrument / Pall Flowstar IV FFS04 Filter Integrity Tester) are precision filter integrity test instruments designed to check whether sterilising-grade membrane filters and associated assemblies have defects (like leaks or incomplete retention) before they are used in critical processes — particularly in pharmaceutical manufacturing and biotech Fpodpfsyfhdmjx Aa Ejd Typical Uses These instruments are most commonly used in environments where sterility is critical: Final filtration before sterile drug product filling. Leak testing of single-use assemblies and filter housings. Quality control in vaccine production, biologics manufacturing, and related biotech workflows.

Condition: new, Year of construction: 2020, functionality: fully functional, Machine designation BRINOX Process System / CIP Skid Type CS6700 (CS6723) GMP CIP Process Skid 1.4435 Manufacturer BRINOX Process Systems Year of manufacture 2020 Technical Data Design as a stainless steel process skid in hygienic execution. Conductivity measurement 1–500 µS/cm, analog signal (AI), hygienic connection DN 50. Flow measurement 0–18,000 kg/h, analog signal (AI), connection DN 25, sterile flange DIN 11864-2A. Pressure measuring points −1 to 9 bar and −1 to 15 bar, analog signal (AI), hygienic connections DN 50 or ½", e.g. DIN EN ISO 228. Temperature measuring points −50 °C to +200 °C, analog signal (AI), connection DN 32, welded according to DIN 11866/A. Limit level sensors, digital (DI), hygienic connection DN 50. Multiple position feedbacks with IO-Link / digital. Pneumatically actuated on/off valves (DO) in stainless steel hygienic design. Product-contact materials according to EN 1.4435 / 1.4404 (AISI 316L). Documented surface roughness of product-contact surfaces Ra approx. 0.3–0.4 µm. Application Hygienic CIP and process plant for pharmaceutical and biotechnological applications. Suitable for cleaning process lines and vessels under GMP conditions. Construction Welded stainless steel skid with orbital welded piping. Hygienic clamp and sterile connections. Fully instrumented with flow, pressure, temperature, and conductivity measurement. Fpodpoyl H Svsfx Aa Ejd Pneumatic valve technology with digital feedback. Components from renowned manufacturers such as Endress+Hauser, Gemü, Samson, SICK, and others. Clean, GMP-compliant execution. Condition New. Original packaging. Unused. Never installed or commissioned. FAT / Documentation Status Fully documented Factory Acceptance Test carried out. Layout drawing inspection documented. Maintenance and calibration accessibility check documented. Surface roughness test documented. Leak test documented. Sensor calibration documented. Welding documentation fully verified. Complete Documentation List FAT plan and FAT report. P&I diagram. Layout drawings. Material lists for metals and polymers. Material certificates 3.1. WPQR, WPS, welder qualifications. Welding protocols and isometrics. Calibration certificates for measuring instruments. Surface roughness measurement protocols. Leak test protocols. EU declarations of conformity for installed components. Operating documentation. Special Features GMP-compliant, fully documented manufacturing. High-quality instrumentation. Very low documented roughness values. Immediately available. Ideal for pharmaceutical, biotech, or contract manufacturers with high documentation requirements.

Condition: new, The Instrument Reprocessing Revolution Careclave can be installed quickly and easily in any reprocessing room. Four process steps in one device – compelling advantages for your practice! Why use four separate instrument reprocessing products when you can have everything in one? With Careclave, you'll save significantly more time, money, and space in your dental practice from day one compared to conventional device combinations: €6,000.00 less in service costs: Because fewer devices mean lower costs. Careclave is not only more affordable to purchase, but it also saves you the extra maintenance and validation costs for additional devices. 45% more space in the reprocessing room: Your practice team knows that workspace in the reprocessing room is valuable. With Careclave, you have significantly more space for the safe reprocessing of your instruments! You can do without an additional care device. 33% more transfer instruments per cycle: Careclave is a real speed demon. Reprocessing eight hollow instruments in just 16–18 minutes guarantees rapid reuse and thus reduces the need for additional instruments. The revolutionary 4-in-1 solution combines the entire instrument reprocessing process in a single device: 1. Cleaning and Disinfection Careclave® ensures the cleaning and disinfection of up to eight handpieces, prophylaxis handpieces, or ultrasonic scaler tips in just 16 minutes. 2. Maintenance Careclave gently and quickly maintains the handpieces in the Carebox. With the world's first integrated ADDcare maintenance station, the crucial chuck maintenance is also performed directly at the Careclave. 3. Sterilization (Class B) With its patented DRYtelligence® and double-jacket technology, the Careclave offers everything you would expect from a modern autoclave – and more: Sterilize up to 11 kg of instruments on up to 8 trays or in 4 MELAstore® boxes in record time. Thanks to the revolutionary chamber design, reprocessing and maintaining instruments in the Carebox, as well as simultaneously sterilizing other instruments on short trays, is possible in a single cycle. 4. Documentation and Release With ProControl, you can provide proof of flawless instrument reprocessing quickly, securely, and paperlessly. Documentation and release are performed directly on the Careclave® display without the need for additional software. For seamless traceability, the reprocessing protocols are saved to the MELAG USB stick or on the practice network. 4. Documentation and Release Model: Careclave 618 Dimensions (D x W x H): 65.3 cm x 48 cm x 56.2 cm Fits a 60 cm tabletop Internal dimensions: Ø 25 cm x 35 cm Area of ​​application: Dental Fpjdpfx Aajyk Eqbj Eod Power supply: 220–240 V, 50 Hz Power consumption: 3 kW Compressed air connection: 4–8 bar Validability: Validatable Sterilization class: Class B Documentation: USB, network Chamber volume: 18 liters Load capacity: 11 kg instruments / 2 kg textiles Suitable for textiles: Yes Suitable for hollow instruments: Yes Suitable for endoscopes: Yes Drying: Integrated drying system Color: White Weight: 69 kg MSRP €21,509.00 Financing through our bank is also available. komplett-konzept.leasingo.de Find more items – new and used – in our shop! International shipping costs on request!

Year of construction: 2023, condition: new, Tuttnauer T-Edge 11 Tabletop Autoclave The fully automatic T-Edge 11 sterilizer is much more than just an autoclave. Your skills are needed in your practice, and your time is a crucial factor. T-Edge therefore frees you from unnecessary effort. Meets stringent international standards Clinically proven applications High-resolution touchscreen Innovative technology Easy-to-use interface Elegant design Excellent user experience Sterilization at the touch of a button Select the desired program and press “Start” The autoclave takes care of everything else – “click and go”. Fpsdpfxjyk D Ede Aa Esd Technical specifications Chamber dimensions Diameter x Length: 280 x 460 mm Chamber volume: 27 liters External dimensions (D x H x W): 500 x 500 x 580 mm Dish dimensions (D x H x W): 421 x 207 x 20.5 mm Power supply: 50/60Hz, 230V-1Ph+N+GND Connections: 1 Ethernet port, 2 USB ports, Wi-Fi, integrated connection for automatic water supply and drainage Weight: 56 kg 0 cycles Year of manufacture: 2023 Financing through our bank is also possible. komplett-konzept.leasingo.de Find more items – new and used – in our shop! International shipping costs on request!

Year of construction: 2023, condition: like new (used), Tuttnauer T-Edge 11 Tabletop Autoclave The fully automatic T-Edge 11 sterilizer is much more than just an autoclave. Your skills are needed in your practice, and your time is a crucial factor. T-Edge therefore frees you from unnecessary effort. Meets stringent international standards Clinically proven applications High-resolution touchscreen Innovative technology Easy-to-use interface Elegant design Excellent user experience Sterilization at the touch of a button Select the desired program and press “Start” The autoclave takes care of everything else – “click and go”. Technical specifications Chamber dimensions Diameter x Length: 280 x 460 mm Chamber volume: 27 liters External dimensions (D x H x W): 500 x 500 x 580 mm Dish dimensions (D x H x W): 421 x 207 x 20.5 mm Power supply: 50/60Hz, 230V-1Ph+N+GND Connections: 1 Ethernet port, 2 USB ports, Wi-Fi, integrated connection for automatic water supply and drainage Weight: 56 kg 58 cycles Year of manufacture: 2023 Financing through our bank is also available. komplett-konzept.leasingo.de Find more items – new and used – in our shop! Fsdpfxjyk A Nus Aa Ejpd International shipping costs on request!

Year of construction: 2010, condition: used, machine/vehicle number: TNK7, Technical Specifications & Performance Data This aseptic storage tank is engineered for hygienic storage and buffering of sensitive liquid food products in beverage production and industrial packaging environments. Manufactured by Tetra Pak in 2010, it is ideal for second hand facilities upgrading or expanding an existing used bottling line with reliable aseptic capacity. Two units are available, each offering substantial storage volume with robust sanitary construction. Type: Aseptic storage tank for liquid food products Manufacturer: Tetra Pak Year: 2010 Nominal capacity (per tank): 13,000 liters Maximum product weight: Construction: High-quality stainless steel, sanitary design Valve system: Cluster valves for controlled, hygienic product flow Quantity available: 2 units (per-tank specification) Application: Aseptic storage of milk, flavored milk, juices, and liquid dairy products Advanced Automation & Control Systems The tank integrates seamlessly into automated aseptic processes. Cluster valves enable precise, automated product routing with minimized contamination risk and simplified cleaning transitions. The design supports CIP (Cleaning-in-Place), ensuring efficient sanitation cycles and repeatable hygienic performance across production shifts. The aseptic configuration is engineered to protect product integrity and maintain sterility from upstream processing through downstream filling and packaging machinery. Production Line Integration Capabilities Fpsdpfx Aaeyhbm Ts Eed This aseptic tank is designed to interface with UHT processing lines, fillers, and other bottling equipment within a used bottling line or new installation. It enables stable buffering between processing and filling, improving uptime and throughput in beverage production. The sanitary connections and cluster valve manifolds simplify tie-ins to existing pipelines and control strategies, facilitating integration into multi-product operations in dairy and juice applications. Machine Condition & Maintenance History These second hand tanks come from a professional food and beverage environment and are presented as ready for operation, consistent with Tetra Pak’s durable hygienic engineering. The aseptic configuration and CIP-ready design support ongoing sanitary maintenance programs and long service life in industrial packaging settings. Operational Performance & Versatility Optimized for liquid dairy and juice products, the tank maintains sterility to help preserve product quality and shelf life prior to filling. The stainless steel construction, sanitary welds, and aseptic valves support stringent hygiene protocols. This configuration is well-suited for producers seeking dependable storage capacity to stabilize production, reduce changeover risks, and align processing cadence with filling schedules across beverage production lines. Installation Requirements & Site Preparation Installation typically requires appropriate floor space, access for piping to upstream/downstream equipment, and utilities compatible with aseptic processes. The tank supports CIP connections for caustic and rinse media, and the valve cluster accommodates ...

Condition: new, Year of construction: 2020, functionality: fully functional, tank capacity: 3,500 l, Equipment: documentation/manual, BRINOX 3,500 L Storage Tank – 1.4404 – PED Module G – TÜV – FAT – 2020 – As New Manufacturer: BRINOX d.o.o., Slovenia Type: SVBBH-3500 Tag no.: Serial number: 1003461 Year of manufacture: 2020 Condition: As new / unused BH6771-BH1001 Package 29 TECHNICAL DATA Product type: Storage tank / process vessel Nominal capacity: 3,500 liters Total volume: approx. 4,082 liters Empty weight: approx. 1,750 kg Material in contact with product: 1.4404 (AISI 316L) Internal surface: electropolished Surface roughness: tested according to roughness protocol (Ra ≤ 0.8 µm) Permissible pressure PS, vessel: -1 / +3 bar Test pressure PT, vessel: 5.6 bar Permissible pressure PS, jacket: -1 / +6 bar Test pressure PT, jacket: 10.8 bar Permissible temperature TS: -10 °C to +150 °C Fluid group: 2 Design according to AD 2000 Pressure vessel according to PED 2014/68/EU Category III Module G – single item inspection CE marking FAT – Factory Acceptance Test Full FAT inspection carried out on 26.08.2020. Documentation check: complete and released Welding documentation inspected and compliant Delta ferrite inspection conducted, no deviations Surface roughness checked and compliant All inspections rated “OK”. EXECUTION • Horizontal cylindrical pressure vessel • Dished heads • Multiple CIP connections on end face • CIP spray ball system • Manhole with round pressure cover • Pressure and temperature connections • Bottom discharge outlet • Stainless steel support legs • Pharmaceutical-grade weld seams DOCUMENTATION – fully available • EU Declaration of Conformity • TÜV certificate • Module G individual inspection • FAT protocols • Welding documentation • WPQR / WPS • 3.1 Material certificates • Non-destructive test reports • Delta ferrite test report • Roughness protocol • Dimensional accuracy report • Calibration certificates • Technical drawings • Parts list • Operating and maintenance manual Complete digital documentation folder available. CONDITION • Never in productive use • Stored item • Interior surface in absolutely as-new condition • No corrosion • No signs of use • As-new industrial condition • Immediately available Fedpfxsylnppo Aa Eopd SUITABLE FOR • Pharmaceutical solutions • WFI / PW systems • Buffer and media preparation • Sterile liquid processes • GMP production facilities • Biotechnological applications SPECIAL FEATURE Custom-manufactured BRINOX pharmaceutical tank with full FAT acceptance, verified welding documentation, delta ferrite certification, documented surface roughness, and comprehensive PED Module G single-inspection. Not a standard tank – but pharmaceutical grade suitable for validation, with complete technical documentation throughout.

Condition: new, Year of construction: 2020, functionality: fully functional, tank capacity: 3,500 l, Equipment: documentation/manual, BRINOX 3,500 L Batch Tank – 1.4435 – Double Jacket – PED Module G – TÜV SÜD – FAT – 2020 – As New Manufacturer: BRINOX d.o.o. Type: SVMBHI-3500 Fpedoylng Uspfx Aa Ejd Tag No.: BH6770-BH1001 Serial number: 1003460 Year of manufacture: 2020 Condition: As new / unused BH6770-BH1001 Package 28 TECHNICAL DATA Product type: Batch tank / pressure vessel Working volume: 3,500 liters Total volume: 4,304 liters Jacket volume: 202 liters Empty weight: 1,958 kg Product contact material: 1.4435 Jacket: 1.4404 CE marking: CE 0036 Permissible vessel pressure PS: -1 / +3 bar Test pressure vessel PT: 5.6 bar Permissible jacket pressure PS: -1 / +6 bar Test pressure jacket PT: 10.8 bar Permissible temperature TS: -10 °C to +150 °C Fluid group: 2 Design according to AD 2000 code Pressure vessel according to PED 2014/68/EU Category III Module G – Individual inspection Notified body: TÜV SÜD Industrie Service GmbH (ID number 0036) TÜV approval including final inspection and pressure test, fully documented. FAT – Factory Acceptance Test The vessel was fully FAT tested and approved at the factory. Tests carried out, among others: • Pressure test per PED • Visual inspection of all weld seams • Non-destructive tests (RT, PT according to test plan) • Dimensional and drawing comparison (as-built) • Internal surface roughness measurement (Ra ≤ 0.8 µm) • Calibration test of manometers • Marking verification • Complete documentation review Full FAT protocols available. DESIGN • Cylindrical, horizontal vessel • Double jacket with half-pipe system • Internally electropolished and passivated • High-gloss product contact surface • Pharmaceutical-grade welds • Manway DN 500 • Powder/product inlet DN 300 • CIP connections • Safety valve • Pressure and temperature connections • Agitator connection • Heavy-duty trunnion supports • Lifting lugs DOCUMENTATION – complete and structured Extensive project-specific quality and manufacturing documentation available, including: • EU Declaration of Conformity and guarantee certificates • TÜV certificate with acceptance report (Module G) • TÜV design review and certification • Material certificates 3.1 • Welder lists and welding procedure qualification records (WPQR/WPS) • Non-destructive test reports (RT, PT, etc.) • Analysis certificates for welding filler materials and gas • Company qualification certificate • Roughness protocol • Surface treatment report • Dimensional accuracy test report • Internal pressure test report • Calibration certificates • Reports and EU conformity of installed components • Parts list compilation • Detail drawings • Operating and maintenance manuals Complete digital documentation package available. CONDITION • Never used in production • Stock item • Interior surface absolutely as new • No corrosion • No signs of use • Industrial new condition • Immediately available SUITABLE FOR • Pharmaceutical solutions • WFI / PW systems • Buffer and media preparation • Sterile liquid processes • GMP production plants • Biotechnological applications SPECIAL FEATURES High-quality BRINOX pharmaceutical fabrication with complete PED Module G individual approval by TÜV SÜD, CE 0036 marking, and fully documented FAT inspection. Not a standard tank – this is audited project quality with comprehensive GMP-compliant documentation.

Condition: new, Year of construction: 2020, functionality: fully functional, tank capacity: 1,500 l, Equipment: documentation/manual, BRINOX 1,500 L Process Vessel – 1.4435 – Double Jacket – PED Module G – TÜV – FAT – 2020 – Like New Manufacturer: BRINOX d.o.o. Tag No.: BH6726-BH1001 Type: SVMBBI-1500 Year of Manufacture: 2020 Serial No.: 1003458 Equipment No.: 20051401 CE Marking: CE 0036 Condition: Like new / unused Empty weight: 866 kg TECHNICAL DATA Product type: Main filling vessel / process vessel Design: cylindrical with dished ends Working volume: 1,500 liters Total volume: 1,785 liters Product-contact material: 1.4435 Jacket material: stainless steel (double jacket design) Max. allowable pressure (PS) vessel: -1 / +3 bar Test pressure (PT): 5.4 bar Max. allowable temperature (TS): -10 °C / +150 °C Pressure vessel in accordance with PED 2014/68/EU Module: G Fluid group: 1 SURFACE & EXECUTION Internal surface: high-gloss polished, pharmaceutical design Product-contact areas made of 1.4435 Weld seams finely ground Pharmaceutical CIP-capable design EQUIPMENT • Double jacket for heating/cooling • Large manway with clamp closures • Multiple instrument and process nozzles • Pressure sensor / temperature connections • Bottom outlet Fpjdpjykuhisfx Aa Ejd • CIP/spray ball connections • Various blank flanges • Insulated media connections on jacket • FDA-compliant seals CONDITION • Never used in production • Stock item • Interior absolutely like new • No corrosion • No signs of use • Immediately available DOCUMENTATION – complete • EU Declaration of Conformity • TÜV acceptance documents • PED Module G documentation • Material certificates 3.1 • Pressure test report (PT 5.4 bar) • Technical drawings • FAT documentation • Operating manual SPECIAL FEATURE Large-volume BRINOX main filling vessel, 1,500 L in 1.4435, PED Category IV Module G, CE 0036, with complete documentation, pharmaceutical-grade surface finish, and pressure test at 5.4 bar. Project quality for sterile applications – immediately available.

Condition: new, Year of construction: 2020, functionality: fully functional, tank capacity: 1,500 l, Equipment: documentation/manual, BRINOX 1,500 L Process Vessel – 1.4435 – Jacketed – PED Module G – TÜV – FAT – 2020 – As New Manufacturer: BRINOX d.o.o. Tag No.: BH6722-BH1001 Year of manufacture: 2020 Condition: As new / unused CE Marking: CE 0036 TECHNICAL DATA Product type: Main/process vessel Design: Cylindrical with dished ends Working volume: 94 – 1,500 liters Empty weight: 866 kg Product contact material: 1.4435 Jacket material: 1.4307 Insulation: yes Operating pressure (vessel): -1 / +3 barg Permissible pressure (PS): -1 / +3 barg Test pressure (PT): 5.4 bar Permissible temperature (TS): -10 °C / +150 °C Date of pressure test: 2020/04 Pressure vessel according to PED 2014/68/EU Category IV Assessment procedure: Module G Notified body: TÜV SÜD Industrie Service GmbH Design code: AD 2000 SURFACES & WELDS Internal surface: Electropolished and passivated Pharmaceutical grade External surface: Industrial ground finish NDT / Inspections: RT (radiographic testing) PT (penetrant testing) Pressure testing documented 2020 EQUIPMENT • Double jacket for heating/cooling • Large frontal manway • Multiple process nozzles • CIP connections • Temperature and pressure ports • Safety fittings • Agitator mount • FDA-compliant seals • Complete piping module CONDITION • Never used in production • Stock item • Internal surface absolutely as new • No corrosion • No signs of use • Available immediately DOCUMENTATION – fully available Fpjdpfjykuc Tjx Aa Ejd • EU Declaration of Conformity • TÜV certificates and inspection reports • PED Module G documentation • Material certificates 3.1 (EN 10204) • Welding logs • NDT reports (RT / PT) • 2020 pressure test report • Surface reports • Detail and assembly drawings • FAT documents • Operating and maintenance manuals SPECIAL FEATURE BRINOX pharma process vessel in 1.4435 with electropolished internal surface, AD2000 design, PED Category IV Module G, full TÜV inspection 2020, and complete technical documentation. Project quality for sterile applications – immediately available.

Condition: new, Year of construction: 2020, functionality: fully functional, tank capacity: 1,000 l, Equipment: documentation/manual, BRINOX 1,000 L Pre-Fill Vessel – 1.4435 – Double Jacket – PED Cat. IV Module G – TÜV – FAT – 2020 – As New Manufacturer: BRINOX d.o.o. Type: SVMMBI-1000 Tag No.: BH6725-BH1001 Serial No.: 1003455 Year of manufacture: 2020 CE Marking: CE 0036 Condition: As new / unused TECHNICAL SPECIFICATIONS Product type: Pre-fill / process vessel Nominal volume: 1,000 L Total volume: 1,400 L Empty weight: 762 kg Product contact material: 1.4435 Permissible pressure (PS): -1 / +3 bar Test pressure (PT): 5.4 bar Permissible temperature (TS): -10 / +150 °C Fluid group: 1 Design according to AD 2000 Pressure vessel compliant with PED 2014/68/EU Category IV Module G – Single Unit Inspection Notified body: TÜV SÜD Notification number: 0036 FAT – Factory Acceptance Test Full factory FAT conducted and documented. Testing includes pressure test, NDT (non-destructive testing), dimensional inspection, surface roughness inspection, and documentation release. FEATURES • Cylindrical horizontal pressure vessel • Double jacket for heating/cooling • Interior electropolished • Pharmaceutical-grade welding • Manway DN500 • Multiple process and instrument connections • Safety valve • CIP connections • Suitable for pressure and vacuum operation CONDITION • Never used in production • TÜV Module G certified • As-new industrial condition • Immediately available DOCUMENTATION – complete and available Comprehensive structured documentation including: • EU Declaration of Conformity • TÜV certificate with inspection report • TÜV design assessment • FAT documentation • Material certificates • Welding lists and WPS/WPQR • NDT reports • Surface roughness protocol • Surface treatment report • Internal pressure test • Dimensional protocol • Calibration certificate (pressure gauge) • Component drawings Fsdpfeykt T Rsx Aa Eopd • Assembly parts list • Operation and maintenance manuals (equipment & components) • Qualification certificates • Analysis certificates for welding consumables and shielding gases Complete digital documentation file available. APPLICATIONS • Pharmaceutical industry • WFI / PW • GMP-compliant plants • Sterile liquid processes • Biotechnology High-quality BRINOX pharmaceutical version with PED Cat. IV Module G single unit inspection by TÜV SÜD, complete FAT, and full technical documentation. Immediately available.

Condition: new, Year of construction: 2020, functionality: fully functional, machine/vehicle number: BH6723-BH1001, tank capacity: 1,000 l, Equipment: documentation/manual, BRINOX 1,000 L Pre-Fill Tank – 1.4435 – Double Jacket – PED Cat. IV Module G – TÜV – FAT – 2020 – As New Manufacturer: BRINOX d.o.o. Type: SVMMBI-1000 Tag No.: BH6723-BH1001 Serial No.: 1003454 Year of Manufacture: 2020 CE Marking: CE 0036 Condition: As new / unused TECHNICAL DATA Product type: Pre-fill / process vessel Nominal volume: 1,000 L Total volume: 1,400 L Net weight: approx. 610–762 kg Product contact material: 1.4435 (AISI 316L) Permissible pressure PS: -1 / +3 bar Test pressure PT: 5.4 bar Permissible temperature TS: -10 / +150 °C Fluid group: 1 Design according to AD 2000 Pressure vessel in accordance with PED 2014/68/EU Category IV Module G – Individual inspection Notified body: TÜV SÜD Identification number: 0036 TÜV CERTIFICATION EU Declaration of Conformity (Module G) Certificate no.: Z-EU-SI-LJU-20-05-2702107-19125214 Inspection report no.: P-EU-SI-LJU-20-05-2702107-19125214 Final inspection in accordance with PED Annex I No. 3.2 carried out Pressure test in accordance with Annex I No. 3.2.2 carried out Acceptance without deviations Permissible load cycle count: 10,000 cycles (1.3 bar) Acceptance date: 20.05.2020 FAT – Factory Acceptance Test Complete works FAT carried out: Fpedpfx Aaoykqmze Ejd • Pressure test • Visual inspection of weld seams • NDT testing (RT/PT) • Dimensional inspection • Surface roughness measurement (≤ 0.8 µm) • Calibration test • Documentation review FAT fully documented. DESIGN • Cylindrical, horizontal pressure vessel • Double jacket for heating/cooling • Internally electropolished • Pharmaceutical-grade weld finish • Manhole DN 500 • CIP connection • Safety valve • Pressure gauge • Multiple process and measuring nozzles • For pressurised and vacuum operation CONDITION • Never used in production • Factory tested • TÜV Module G certified • As-new industrial condition • No signs of use • Immediately available DOCUMENTATION Complete structured documentation available, including: • EU Declaration of Conformity • TÜV certificate with inspection report • TÜV design assessment • FAT protocols • Material certificates EN 10204 3.1 • WPS/WPQR and welders’ lists • NDT reports • Surface roughness protocols • Internal pressure test • Measurement reports • Calibration certificates • Parts list and drawings • Operating and maintenance manuals Digital documentation folder available. • Pharmaceutical solutions • WFI / PW systems • Buffer and media preparation • Sterile liquid processes • GMP installations • Biotechnology High-quality BRINOX pharmaceutical specification with PED Cat. IV Module G individual inspection by TÜV SÜD (CE 0036) and complete FAT documentation. Not a standard tank – tested project quality. Immediately available.

Condition: new, Year of construction: 2020, functionality: fully functional, machine/vehicle number: BH6721-BH1001, tank capacity: 1,000 l, Equipment: documentation/manual, BRINOX 1,000 L Pre-Filling Tank – 1.4435 – Double Jacketed – PED Module G – TÜV SÜD – FAT – 2020 – As New Manufacturer: BRINOX d.o.o. Type: SVMBBl-1000 Tag No.: BH6721-BH1001 Serial No.: 1003453 Year of Manufacture: 2020 Condition: As new / unused TECHNICAL DATA Product type: Pre-filling tank / process vessel Nominal volume: 1,000 liters Total volume: 1,400 liters Empty weight: 762 kg Product-contact material: 1.4435 (AISI 316L pharmaceutical grade) CE Marking: CE 0036 Permissible pressure PS: -1 / +3 bar Test pressure PT: 5.4 bar Permissible temperature TS: -10 °C to +150 °C Fluid group: 1 Design according to AD 2000 code Pressure vessel in accordance with PED 2014/68/EU Category IV Module G – Individual inspection Notified Body: TÜV SÜD Industrie Service GmbH (ID No. 0036) TÜV acceptance including final inspection and pressure test fully documented. FAT – Factory Acceptance Test Fedpfxsykpqrs Aa Eepd The vessel underwent full FAT testing and approval at the manufacturer’s site. Tests carried out include: • Pressure test in accordance with PED • Visual inspection of all weld seams • Non-destructive testing (RT, PT as per test plan) • Dimensional and drawing check (as-built) • Internal roughness measurement (Ra ≤ 0.8 µm) • Calibration test of pressure gauges • Verification of markings • Complete documentation review FAT protocols fully available. DESIGN FEATURES • Cylindrical, horizontal tank • Double jacket for heating/cooling • Internally electropolished and passivated • High-gloss product contact surface • Pharmaceutical-grade weld seams • Manhole DN 500 • CIP connections • Safety valve • Pressure gauge • Bottom diaphragm valve • Agitator port (DN 200) • Multiple spare ports • Heavy-duty trunnion/pivot bearing • Transport and lifting devices DOCUMENTATION – fully complete and well structured Comprehensive, project-specific quality and manufacturing documentation available, including: • EU Declaration of Conformity and warranty certificates • TÜV certificate with acceptance report (Module G) • TÜV design test and certification • 3.1 material certificates • Welder lists and welding procedure qualifications (WPQR/WPS) • Non-destructive testing reports (RT, PT, etc.) • Analysis certificates for welding consumables and gases • Company qualification certificate • Roughness protocol • Surface treatment report • Dimensional accuracy report • Internal pressure test report • Calibration certificates for pressure gauges • Reports and EU conformity of installed components • Parts list assembly • Component drawings • Operating and maintenance manuals Complete digital documentation portfolio available. CONDITION • Never used in production • Stock item • Internal surface absolutely as new • No corrosion • No signs of use • As-new industrial condition • Immediately available SUITABLE FOR • Pharmaceutical solutions • WFI / PW systems • Buffer and media preparation • Sterile liquid processes • GMP production plants • Biotechnological applications SPECIAL FEATURE High-quality BRINOX pharma-manufacturing with complete PED Module G individual acceptance by TÜV SÜD, CE 0036 marking, and full FAT test documentation. Not a standard tank, but a quality project vessel with comprehensive GMP-compliant documentation. Immediately available.