Used Gmp Qtopic380 for sale (127)

Condition: used, This listing is for the Akta crossflow filtration system The unit is in full working condition and is ready for immediate use An ÄKTA Crossflow filtration system is a type of tangential flow filtration (TFF) system developed by Cytiva (formerly GE Healthcare). It's used primarily in bioprocessing and biotechnology applications to concentrate, diafilter, or clarify biological samples such as proteins, viruses, plasmids, and other biomolecule Core Functions: Concentration – Reducing the volume of a sample while retaining the target biomolecule. Diafiltration (Buffer Exchange) – Removing salts or changing the buffer environment by continuously adding a new buffer while removing permeate. Clarification – Removing particulates or cells from process fluids Key Components: Pump Modules: Typically peristaltic pumps that manage flow rates precisely. Filtration Cassettes: Hollow fiber or flat sheet membranes for ultrafiltration or microfiltration. Pressure Sensors: To monitor and control transmembrane pressure (TMP). Conductivity/pH/UV Detectors: For in-line monitoring of the filtrate and retentate. Benefits: Automation reduces operator error and variability. Scalable design for seamless transition from lab to production. Precise control of filtration parameters (flow rate, pressure, volume). CIP (Clean-In-Place) capabilities for easy maintenance and compliance with GMP. Common Applications: Protein concentration and buffer exchange Viral vector purification Bodoxhf A Repfx Al Iewl Plasmid DNA purification Cell harvest and clarification

Year of construction: 2018, condition: used, This listing is for a GE Healthcare UniFlux 120 Tangential Flow Filtration (TFF) System. Bedpfx Aexxx Inol Ijwl The unit is in full working condition and ready for immediate release. The GE Healthcare UniFlux 120 is a fully automated Tangential Flow Filtration (TFF) system designed for clarification, concentration, and diafiltration applications in pilot to manufacturing-scale operations. With a flow rate range of 12 to 120 liters per minute, the UniFlux 120 is ideal for bioprocessing applications such as monoclonal antibody purification, vaccine production, and protein concentration. Key Features & Benefits - Fully Automated Operation – The system is controlled by UNICORN software, ensuring seamless data logging, process automation, and compliance with regulatory standards - Versatile Filtration Options – Supports cassette or hollow fiber membranes. Conversion between formats is possible, with initial cassette holder installation requiring Cytiva Service. - High-Performance Filtration – Features a rotary lobe pump for precise flow control and optimized filtration efficiency. - Sanitary & GMP-Compliant Design – Constructed from stainless steel, making it suitable for pharmaceutical and biotechnology environments. - Scalability & Reliability – Designed to support process development and scale-up to commercial production, ensuring consistent filtration performance. Applications - Biopharmaceutical processing - Monoclonal antibody purification - Vaccine production - Protein concentration & buffer exchange - Cell culture clarification Technical Specifications - Flow Rate: 12 – 120 L/min - Pump Type: Rotary lobe pump - Filtration Format: Cassette & hollow fiber (conversion possible) - Control System: UNICORN software (FDA 21 CFR Part 11 compliant)

Condition: used, This listing is for a Sartorius YCW623 2KG / F1 Weight. The unit is in full working condition and is ready for immediate release. The Sartorius YCW623 2kg Knob Weight is a high-precision meteorological weight designed for use in laboratory and industrial settings. It meets OIML Class F1 standards, ensuring accuracy for calibrating balances and scales. Made of highly polished, non-magnetizable stainless steel, this weight is highly corrosion-resistant, making it durable and reliable in various environments. With a density of 8.0 g/cm³, it is ideal for labs requiring strict adherence to quality control protocols such as GLP and GMP. Key Features: OIML F1 classification for precise calibration Material: Polished stainless steel, non-magnetizable, and corrosion-resistant Nominal mass: 2kg Supplied in a protective case for safe handling and storage Bwsdpfxoxx Ap Nj Al Iel This weight is ideal for use in laboratories requiring high precision and compliance with international standards.

Condition: used, System Overview A complete, cGMP-compliant Water for Injection (WFI) generation and storage system. Produces high-purity, endotoxin-free water for pharmaceutical and biotech applications via multiple-effect distillation. This item can be crated and shipped internationally. Please contact us for a quotation ----- Main Components - Finn-Aqua 200-S3 Distillation Unit – three-effect evaporator/condensers with falling-film design, pyrogen separation, and continuous blowdown. - 600 L WFI Storage Tank – 316L stainless steel, atmospheric vent filter, level and temperature sensors. - 600 L Jacketed Holding Tank – 316L stainless steel, insulated, steam/hot water jacket for temperature control. - WFI Distribution Pump – sanitary centrifugal pump for loop circulation. - Utility Connections – plant steam (3–8 bar), cooling water, feed water, condensate return, and instrument air. - Instrumentation – pressure, temperature, conductivity, and level transmitters with safety and relief valves. - Control Panel – PLC-based automatic operation, alarm handling, data logging, and local/remote control. ----- Key Features - Multi-effect distillation for high purity and energy efficiency. - Degassing and three-stage separation for endotoxin removal. - Fully stainless, drainable, and sanitary construction. - Compact, skid-mounted design with integrated utilities. Bwodpfsxqq Dxsx Al Iel - Designed for validation and GMP compliance (USP/EP WFI quality).

Condition: used, This listing is for a Pharmagraph S1816 Particle Counter (1 of 8) The unit is in full working condition and is ready for immediate release. The S1816 series is a continuous-monitoring airborne particle counter designed for use in pharmaceutical cleanrooms, isolators, filling suites and similar controlled environments. It is built by Pharmagraph (UK) and intended to meet stringent regulatory/clean-room requirements (e.g., for EU GMP Annex 1 compliance). The unit houses a laser-based sensor (in particular a Met One 6015 sensor) in a stainless-steel enclosure, intended for permanent monitoring rather than portable spot checks Bwjdpoxtnquofx Al Iol

Condition: used, This listing is introducing 8 No Envair Mobile Isolators of different specifications currently held in our stock The units are in full working condition and ready for immediate use Envair Mobile Isolator Envair Technology is a UK-based manufacturer specializing in clean air and containment solutions for the healthcare, biotechnology, and pharmaceutical industries. Their product range includes a variety of isolators designed to provide controlled environments for handling hazardous substances, ensuring both operator and product safety. Applications Bwedpfxoxv Dhbj Al Iel Envair isolators are widely used in a variety of applications including Hospital Pharmacies: For preparation of TPN, CIVAS, and aseptic dispensing. Pharmaceutical Laboratories: Handling of HPAPIs and sterile compounding. Sterility Testing: Secure, controlled environments for product testing. R&D Facilities: Safe containment during experimental or early-stage developmen Key Features of Envair Isolators Positive and Negative Pressure Models: Envair offers both positive pressure isolators protect the product from contamination and negative pressure isolators to protect the operator from hazardous substances Compliance with GMP Standards: Many Envair isolators meet EU GMP Grade A and ISO 5 classifications, ensuring sterile, controlled environments. Customizable Designs: Envair provides bespoke solutions tailored to specific client needs, including unique dimensions and technical requirements. Advanced Containment Technology: Isolators are equipped with automated pressure decay leak tests, electromagnetic interlocks for transfer chambers, and integrated decontamination systems. User-Friendly Controls: Most units include intuitive touchscreen interfaces and PLC-based systems for simple and efficient operation. Growing Need for Containment with HPAPIs Demand for personalised medicines containing High Potent Active Pharmaceutical Ingredients (HPAPIs)—particularly in newer super-potent oncology, cardiovascular, and diabetes treatments—is increasing rapidly. These medicines often require shorter turnaround times, forcing pharmaceutical process manufacturers to develop faster, more agile workflows. In such high-risk, high-value settings, a GMP-compliant environment is not optional—it’s critical. It’s easy to overlook the fact that the people developing, manufacturing, and dispensing these complex drugs are at risk of exposure to harmful, sometimes lethal, compounds. Their safety is paramount, given the essential role they play in maintaining a reliable supply of advanced therapeutics. Expertise in HPAPI Handling for CMOs & CDMOs Envair has specialist expertise in helping Contract Manufacturing Organisations (CMOs) and Contract Development and Manufacturing Organisations (CDMOs) safely handle HPAPIs—even within existing non-contained facilities. Their isolator systems are designed, manufactured, and installed to meet rigorous containment performance levels below 1μg/m³ (OEB 5). Each system is custom-engineered for the specific site and process step—whether it’s weighing, mixing, milling, spray drying, or packaging. Applications Hospital Pharmacies: For preparation of TPN, CIVAS, and aseptic dispensing. Pharmaceutical Laboratories: Handling of HPAPIs and sterile compounding. Sterility Testing: Secure, controlled environments for product testing. R&D Facilities: Safe containment during experimental or early-stage development

Condition: used, This listing is for 1 of 2 Rainin LTS E4XLS, 5-50µL 8 Channel Pipette The unit is in full working condition and is ready for immediate use This listing is for the The unit is in full working condition and is ready for immediate use Features Electronic multichannel pipette with variable nozzle spacing (9 – 14 mm), ideal for flexible plate formats Volume range: 5–50 µL (recommended operational adjustments via precise joystick control) Bwedpfx Alexv Dtwj Iol LiteTouch System (LTS): dramatically reduces tip ejection force (~85% less), minimizing repetitive strain Jet‑set display & joystick UI with on‑board memory for protocols, password protection, and service alarms Integrated RFID chip supports fleet management, calibration logging, and GLP/GMP compliance Rechargeable battery, USB or cradle charging; settings persist in non‑volatile memory

Condition: used, This listing is for the Amersham Pharma 35L BPG Cromatography Column The unit is in full working condition and is ready for immediate use Bodpfx Aloxhdw Hj Iswl BPG stands for Bio‑Process Glass or BioProcess Glass (sometimes called BPG columns). They are process‑scale chromatography columns used in biopharmaceutical / downstream protein purification. Originally from Amersham / Pharmacia, now under GE Healthcare / Cytiva brands. Made to be hygienic, scalable, reproducible, for use in situations where high cleanliness, sterility, and regulatory compliance matter (e.g. GMP) A BPG column (short for BioProcess Glass column) is a process-scale chromatography column designed specifically for downstream purification in biopharmaceutical manufacturing — particularly for the purification of proteins, antibodies, and other biologics

Condition: used, This listing is for 1 of 2 BWT LOOPO WFI Storage and Distribution System. The unit is in full working condition and is ready for immediate release. Overview This BWT LOOPO system is a high-performance Water for Injection (WFI) storage and distribution solution, designed for reliable and hygienic operation in pharmaceutical and biotech environments. Mounted on a robust stainless steel skid, the unit includes a high-grade stainless steel storage tank, engineered for ambient temperature WFI applications. The system features Siemens HMI controls for intuitive operation and precise system monitoring. Key Features - WFI Storage & Distribution at Ambient Temperature - 30 kW Power Capacity - Siemens HMI Touchscreen Interface - Fully skid-mounted for compact and efficient installation - Stainless steel construction throughout – skid and tank - Ideal for pharmaceutical-grade applications - Designed for continuous circulation to prevent stagnation and microbial growth Bwodpexhdxwsfx Al Iel Technical Specifications - System Type: Ambient WFI Storage & Loop - Construction: Stainless Steel (Skid & Tank) - Control System: Siemens HMI - Power Supply: 30 kW - Installation Type: Skid-Mounted - Year of Manufacture: 2016 Applications - Pharmaceutical manufacturing - Biotech production facilities - Cleanroom and GMP environments - Laboratories requiring sterile WFI distribution

Condition: used, This listing is for a Sartorius MSA4202S 8.2g-2500g Precision Balance Bjdpfxoxuu Hle Al Iowl The unit is in full working condition and is ready for immediate release. Modular design (part of the Cubis® series) – the system is built of a weighing module + display/control unit + interface modules, designed for flexible configuration. High-resolution colour TFT display + touchscreen interface, offering an intuitive user interface. Multiple interfaces standard: USB, Ethernet, RS-232, SD card reader for data transfer and traceability. Functions typically include: weighing, density determination, averaging, formulation, percentage-weighing, check-weighing, totalising. Assisted (and optionally motorised) levelling; the system detects inclination and assists the user in levelling the instrument. Automatic internal calibration (isoCAL) for improved stability and lower drift. GLP/GMP/traceability ready: audit trail functions, user profiles, etc

Condition: used, This listing is for the MMM Group Vakulab HL Medical Autoclave. The unit is in full working condition and is ready for immediate use. Bsdpoxv Dvfjfx Al Iswl 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 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). The chamber is constructed from AISI 316L stainless steel, ensuring corrosion resistance and compliance with GMP hygienic standards. A water-ring or liquid-ring vacuum pump enables pre-vacuum and post-vacuum phases for thorough air removal and effective drying. Door configurations can be single or double-door in either sliding or hinged formats, with safety interlocks to prevent opening under pressure. The autoclave requires standard utility connections for 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 Flexible Confi...

Condition: used, This listing is for a GE Axichrom Master 300-1000 Control Tower + GE AxiChrom 300/300 mm Chromatography Column. The unit is in full working condition and is ready for immediate release. The GE AxiChrom Master 300-1000 Control Tower and GE AxiChrom 300/300 mm Chromatography Column offer an advanced, scalable solution for automated column packing in biopharmaceutical purification and process development. Designed for seamless integration and ease of operation, this system enhances workflow efficiency, optimizes chromatography resin performance, and supports GMP compliance for manufacturing applications. Key Features: GE AxiChrom 300-1000 Master Control Tower: Automated Column Control: Preprogrammed methods for packing, unpacking, priming, and maintenance to improve uptime. Touch Screen Interface: Easy-to-use operator interface for precise control. Integration with UNICORN & Automation Systems: Supports Profibus integration with UNICORN or DeltaV Distributed Control System for batch record tracking and regulatory compliance. Multi-Column Management: A single AxiChrom Master unit can control up to ten chromatography columns. Intelligent Packing Wizard: Guides automated priming, packing, and unpacking of chromatography columns. GE AxiChrom 300/300 mm Chromatography Column: Automated Column Packing: Ensures verified packing methods for efficient resin performance. Scalable Design: Adaptable from process development to full-scale production. Optimized for Modern Chromatography Resins: Supports cutting-edge purification techniques. Easy Sanitization: Designed for GMP environments, ensuring safe and sterile operation. Closed-System Connectivity: Can integrate with slurry tanks and chromatography systems for improved process control. Specifications: Column Model: GE AxiChrom 300/300 mm Column Diameter: 300 mm Column Height: 300 mm Voltage: 415V Hertz: 50Hz/60Hz Control Tower Model: GE AxiChrom Master 300-1000 Width: 670 mm Depth: 630 mm Height: 1090 mm Bedpfsxxycajx Al Iswl Foot Print: 630 x 670 mm Weight: 90 kg EMC: IEC/EN 61326-1, Emission according to CISPR 11, Group 1, class A, CFR 47 FCC Part 15B, class A Voltage: 380 - 480 V Frequency: 50/60 Hz Air Supply: 5.5 - 7 bar g. Clean dry air Benefits: Automated & Efficient: Reduces manual intervention, improving process consistency and productivity. Scalable & Flexible: Ideal for process development and full-scale biomanufacturing. Regulatory Compliance: Designed for GMP environments with complete regulatory documentation. Seamless Integration: Connects to UNICORN software, DeltaV, and other automation systems. Multi-Column Control: One AxiChrom Master can manage up to 10 chromatography columns. Applications: This system is ideal for biopharmaceutical purification, including: Monoclonal Antibody (mAb) Production Vaccine & Biologic Drug Manufacturing Recombinant Protein Purification Gene Therapy & Cell Therapy Processing With its combination of automated control, intelligent packing, and scalable chromatography, the GE AxiChrom Master 300-1000 Control Tower + GE AxiChrom 300/300 mm Chromatography Column is a powerful asset for biopharmaceutical manufacturing and large-scale purification applications.

Condition: used, This listing is for an Eppendorf BioFlo 320 Glass Vessel Bioreactor 5L SS Dished Bottom M1379-1001 The unit is in full working condition and is ready for immediate release Bwodpfoxv D Ihjx Al Ijl Key Features Material: Autoclavable borosilicate glass vessel with a stainless steel headplate. Bottom Design: Dished stainless steel bottom for rapid heat transfer. Drive Options: Compatible with both magnetic and direct overhead drive systems. Impeller Options: Supports various impellers including Rushton, pitched blade, marine blade, spin filter, cell lift, and packed-bed impellers. Port Configuration: Multiple industry-standard headplate ports for flexibility in process design. Temperature Control: Suitable for both rapid and gentle temperature control processes.​ Applications This bioreactor is ideal for applications such as:​ Cell culture and microbiology research. Laboratory and pilot-scale fermentation of aerobic and anaerobic bacteria, yeasts, and fungi. Cultivation of mammalian, insect, and human cell lines. Specialized applications like stem cell culture or biofuel/biopolymer development. Packed-bed impeller use for vaccine production in anchorage and non-anchorage dependent cell lines. Suitable for batch, fed-batch, and continuous processes. Validation packages available for GMP-regulated processes

Condition: used, This listing is for the Cytiva AxiChrom 300/300 Chromotography collumn The unit is in full working condition and is ready for immediate use Bsdjxhdwyepfx Al Iowl AxiChrom is a line of low-pressure, axial compression chromatography columns designed for process development and manufacturing of biopharmaceuticals. They are built for GMP‐compatible use, scalable from lab/ pilot to full production 300 mm inner diameter (i.d.) 300 mm bed height (column length) or related bed volume configuration Features Axial compression packing (intelligent packing): preprogrammed / automated methods for packing, ensuring reproducible bed density / performance. “Swing‑out” tube or movable adapters: for large diameters (≥ 300 mm), the column tube swings out to allow easier access to the bed supports, seals and O‑rings. Sanitization / Cleaning / GMP compliance: Parts (“wetted” and “pressure retaining”) are traceable by batch, and materials comply with USP Class VI, 21 CFR part 177, EMEA regulatory requirements. Cleaning and sanitization are feasible, including treatment with 1 M NaOH, with effectiveness for microbial and endotoxin removal. Flexible configurations: options for different bed heights (usually ~10‑50 cm for large diameters) and different bed support types

Condition: used, This listing is for the Partical Measuring Systems LASAIR lll 310c particle measuring systems The unit is in full working condition and is ready for immediate release The Lasair® III 310C is a state-of-the-art portable aerosol particle counter designed to meet the stringent requirements of highly regulated environments. Manufactured by Particle Measuring Systems (PMS), it sets the standard for portable particle counters, ensuring that your environment remains clean and compliant.​ Key Features Bsdpfxjxv A T Nj Al Iswl Particle Size Range: 0.3 to 25.0 µm Flow Rate: 1.0 CFM (28.3 LPM) ±5% Counting Efficiency: Complies with ISO 21501-4 requirements Display: 8.4" color VGA IR touch screen (IP65 rated) Data Storage: Up to 3,000 complete data sets Connectivity: Ethernet, Modbus TCP/IP, RS-232, USB data downloading; optional wireless Ethernet Environmental Inputs: Four 4-20 mA inputs for external sensors Power Options: Operates on AC power or hot-swappable batteries Compliance: Meets ISO 14644-1, EU GMP Annex 1, and ISO 21501-4 standards Software Compatibility: Supports FacilityNet, PharmaceuticalNet, and FacilityPro for data analysis and reporting Reporting Capabilities: Cleanroom certification results are available through a local printout, downloadable via USB in a secure format, or through the use of external software packages Wireless Communication: Wireless network communications are facilitated with an externally mounted wireless adapter, simplifying communications with network systems ​ Specifications Dimensions: 30.1 x 32.7 x 25.9 cm Weight: 6 kg (without battery), 7.5 kg (with two optional batteries) Operating Environment: Temperature: 0 – 30°C; Humidity: 5 – 95% RH non-condensing Sample Tubing: Supports 3/8", 1/2", and 3/4" tubing up to 8 meters in length Sample Output Filtering: Internally filtered to >99.97% at 0.3 µm

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. Bedsxhflxspfx Al Ijwl 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 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: new, Year of construction: 2020, functionality: fully functional, Equipment: documentation/manual, Package 15 PP6715 – CS6715 Brinox LEP 11 – Pharma Chromatography and CIP System New – original packaging – Factory New Manufacturer: Brinox Model: LEP 11 Version: PP6715 with CIP System CS6715 Condition: New, unused, original packaging Description For sale is a high-quality pharmaceutical chromatography system Brinox LEP 11, consisting of the PP6715 control panel and the corresponding CS6715 CIP unit. The system is completely new, unused, and in the manufacturer's original condition. It was designed for industrial C1-INH chromatography and meets the highest GMP standards. Scope of Functions - Slurry transfer - Washing and elution processes - Transfer to pre-precipitation tanks - Gel disposal - Independent CIP loop Technical Features - Product-contacting components in stainless steel 1.4435 - Electropolished, Ra ≤ 0.8 µm - FDA-compliant sealing systems - CIP/SIP-capable - Operating pressure up to 6 bar - Temperature range up to 95°C - Fully drainable piping CIP Skid CS6715 - Stainless steel frame Bwedpfx Aleyl Rqpo Ijl - Centrifugal pump - Shell-and-tube heat exchanger - Temperature control of cleaning media - Adjustable feed pressure The system is in factory-new condition with zero operating hours.

Year of construction: 2020, condition: new, functionality: fully functional, Equipment: documentation/manual, Package 14 PP6713 – CS6713 Brinox LEP 11 – GMP Chromatography System with CIP Skid New – unused – in original packaging Bwsdpfx Aleyl Rnnj Ijl Manufacturer: Brinox Model: LEP 11 Version: PP6713 with CIP System CS6713 Condition: New – in original packaging – never installed Description Offered is a pharmaceutical chromatography system LEP 11, consisting of the chromatography panel PP6713 and the corresponding CIP skid CS6713. The system is completely new, unused, and remains in the manufacturer’s original condition. The unit was designed for GMP-grade protein purification as part of C1-INH chromatography. System Features Cleanroom panel for wall integration Transfer lines to sieve-bottom tanks Precipitation vessel connection Gel waste disposal line Complete utility/process piping Technical Specifications Design pressure: –0.9 to +6 bar Design temperature: +2 to +95 °C Electropolished surfaces Ra ≤ 0.8 µm Material: 1.4435 stainless steel Fully drainable GMP-compliant design CIP System CS6713 Stainless steel frame construction Centrifugal pump Shell-and-tube heat exchanger Conductivity, pressure, and temperature monitoring Adjustable CIP supply flow The system is brand new and has never been in operation.

Condition: new, Year of construction: 2020, functionality: fully functional, Equipment: documentation/manual, Brinox LEP 11 – Pharmaceutical Chromatography System with CIP Unit New, unused, original packaging Manufacturer: Brinox Model: LEP 11 Version: PP6711 with associated CIP unit CS6711 Condition: New – unused – original packaging (Factory New Condition) Description For sale is a Brinox LEP 11 pharmaceutical chromatography system, consisting of the chromatography panel PP6711 and the associated CIP unit CS6711. The system is completely new, unused, and in its original packaging. It was designed, manufactured, and delivered, but has never been installed or put into operation. This unit is designed for C1-INH chromatography and is used for controlled protein purification using sieve-bottom vessels in a GMP environment. Process Functions • Transfer of loaded QAE resin (slurry) • Washing and elution processes • Transfer of eluate to pre-precipitation vessel • Gel disposal via container station • Fully automatic CIP and SIP cleaning Technical Data • Fully CIP and SIP capable • Design pressure: –0.9 to +6 bar • Design temperature: +2°C to +95°C • Flow rate up to 10 m³/h • Adjustable slurry transfer 0.2 – 3 m³/h Bwedpfxjyl Ndnj Al Iol Design Features • Product-contact parts made of stainless steel 1.4435 • Electropolished Ra ≤ 0.8 µm • FDA and EU-compliant seals • Drainable construction • Cleanroom panel with tri-clamp connection points • Magnetically monitored transfer arcs • 0.2 µm vent filter CIP Unit CS6711 • Compact stainless steel skid • Centrifugal pump • Shell-and-tube heat exchanger • Adjustable operating pressure • GMP-compliant design The system is in factory-new condition and has never been used in production.

Condition: new, Year of construction: 2020, functionality: fully functional, tank capacity: 3,500 l, Equipment: documentation/manual, BRINOX 3,500 L Storage Tank – 1.4435 – Double Jacket – PED Module G – TÜV SÜD – FAT – 2020 – Like New Manufacturer: BRINOX d.o.o. Type: SVBBHI-3500 Tag No.: BH6772-BH1001 Package 30 Serial Number: 1003462 Year of Manufacture: 2020 Condition: Like new / unused TECHNICAL DATA Product Type: Storage / Process Tank Nominal Volume: 3,500 litres Total Volume: 4,082 litres Jacket Volume: 226 litres Empty Weight: approx. 1,760 kg Product-contacting Material: 1.4435 (AISI 316L pharmaceutical grade) Jacket Material: 1.4404 CE Marking: CE 0036 Permissible Pressure PS (Tank): -1 / +3 bar Permissible Pressure PS (Jacket): -1 / +6 bar Test Pressure PT (Tank): 5.6 bar Test Pressure PT (Jacket): 10.8 bar Permissible Temperature TS: -10 °C to +150 °C Fluid Group: 2 Designed in accordance with AD 2000 regulations Pressure vessel according to PED 2014/68/EU Category IV Module G – Individual Inspection Notified Body: TÜV SÜD Industrie Service GmbH (ID No. 0036) TÜV approval including design review, final inspection and pressure test fully documented. FAT – Factory Acceptance Test The vessel has been fully inspected and released by the manufacturer. Tests carried out include: • Pressure test as per PED • Design review by TÜV SÜD • Visual inspection of all weld seams • Non-destructive testing (RT, PT) • Dimensional and drawing check (as-built) • Review of material certificates • Calibration check of manometers • Verification of markings • Documentation review as per inspection checklist Bedpfx Ajylnwysl Iswl Full FAT and TÜV inspection reports available. EXECUTION • Cylindrical, horizontal storage tank • Double jacket for heating/cooling • High-quality pharmaceutical design • Manhole with round pressure closure • CIP pipework • J-pipe / internal piping • Sight glass DN80 • Multiple spare and process connections • Biocontrol flanges • Heavy-duty mounting blocks / trunnion design • Lifting lugs • Nameplate with complete PED marking DOCUMENTATION – complete and well-structured • EU declaration of conformity • TÜV certificate with inspection report (Module G) • TÜV design assessment and certification • 3.1 material certificates • Welder lists and work samples • Non-destructive test reports (RT, PT) • Dimensional inspection reports • Manometer calibration reports • Surface and production reports • Parts list • Detailed drawings (body, lid, CIP, J-pipe, etc.) • Operating and maintenance manuals Complete digital documentation folder available. CONDITION • Never put into operation • Was in storage • Interior surface 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 • Chemical media • GMP production facilities • Process and waste management plants SPECIAL FEATURE Premium BRINOX pharmaceutical-grade manufacture with full PED Module G individual inspection by TÜV SÜD, CE 0036 marking and documented FAT testing. Not a standard tank – certified project quality with comprehensive GMP-compliant documentation.

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 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) Bwodpfeylng Ujx Al Iol • 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, 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) Bwodpfx Aleykqmzs Iol 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: • 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 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. Bodpfxsykpqro Al Iewl 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.

Condition: new, Year of construction: 2020, functionality: fully functional, tank capacity: 30,000 l, Equipment: documentation/manual, BRINOX 30,000 L WWAS / Solution Tank – 316L – PED – FAT – Complete GMP Documentation – incl. Saddle Supports – 2020 – Like New Manufacturer: BRINOX d.o.o. Tag No.: LV6456-BH1001 Serial No.: 1003464 Year of Manufacture: 2020 Condition: Like new / unused Location: Europe LV6456-BH1001 Package 66 TECHNICAL DATA Product type: WWAS / solution tank / pharmaceutical process vessel Working volume: 30,000 liters Total volume: 33,213 liters Product contact material: Stainless steel 1.4404 (AISI 316L) Surface finish: Chemically pickled, passivated and cleaned Surface roughness: Ra < 1.6 µm Standards and guidelines: • PED 2014/68/EU compliant • CE marking available • GMP-compliant pharmaceutical design Pressure data: Min.: –0.14 bar(g) Max.: +0.5 bar(g) Test pressure: 0.72 bar(g) Temperature range: –20°C to +50°C Hydrostatic pressure test performed. FAT – Factory Acceptance Test Fully documented FAT carried out including: • Dimensional, visual, and identification inspection • Weld seam testing and NDT • Pressure test according to PED • Testing of all connections • Documentation and quality inspection FAT successfully completed. FAT report available. DESIGN / CONSTRUCTION • Horizontal pharmaceutical process vessel • Stainless steel 316L, pharmaceutical grade • Interior surface pickled and passivated • Hygienic, GMP-compliant construction Connections include: • Manway DN500 • Inlet DN100 • Outlet DN50 Bwsdpfxjykngfj Al Iel • Measuring, safety, and process connections Mechanical configuration: • Original BRINOX stainless steel saddle supports included • Heavy-duty design • Lifting points for crane handling present CONDITION • Absolutely as new • Never installed or used in production • Never filled with product • No corrosion or signs of use • Original industrial packaging available • Immediately available Saddle supports are also as new and included in delivery. DOCUMENTATION – fully available (GMP-compliant) Extensive manufacturer and project documentation including: • EU Declaration of Conformity and CE documentation • PED certificates • Material certificates EN 10204 – 3.1 • Welding documents (WPS/WPQR, welder lists) • NDT inspection reports • FAT protocol and pressure test report • Roughness and surface protocols • Calibration certificates • Part drawings and parts lists • Operation and maintenance manuals Documentation fully available in digital form. TRANSPORT AND PACKAGING • Professional export packaging provided • Original industrial packaging • Crane handling possible without issues • Worldwide shipping possible SUITABLE FOR • Pharmaceutical industry • Biotechnology • WWAS, WFI, and PW systems • Sterile process solutions • GMP production plants SPECIAL FEATURE Project surplus from an international pharmaceutical new-build project with complete FAT, PED compliance, and GMP documentation. Large-capacity BRINOX 30,000 L pharma process vessel in as-new installation quality, incl. saddle supports – immediately available.

Condition: new, Year of construction: 2020, functionality: fully functional, tank capacity: 9,000 l, Equipment: documentation/manual, BRINOX 9,000 L Wash Solution Tank – 316L – Jacketed – TÜV / PED – As New Manufacturer: BRINOX d.o.o. Tag No.: BH6751-BH1001 Package 31 Year: 2020 Condition: As new / unused Technical Data Product type: Wash solution tank Nominal volume: approx. 9,000 litres Wetted material: 1.4404 (AISI 316L) Design: Horizontal layout CE marking: available Pressure vessel in accordance with PED 2014/68/EU TÜV-inspected with acceptance report Jacket for heating/cooling available Designed for pharmaceutical applications Internal surface: • High-gloss polish • Pharmaceutical-grade weld seams • Documented surface quality Design / Equipment • Custom-built in 316L stainless steel • Large manway with pressure closure • Integrated CIP spray nozzles / cleaning pipes • Multiple clamp and flange connections • Instrument ports (pressure, temperature, sensors) • Robust lifting and carrying lugs • Heavy-duty industrial design • Pre-installed external piping and process connections • Excellent accessibility for maintenance and inspection The images clearly show the high-quality workmanship, the clean welding, and the mirror-polished product-contact internal surface. Condition Bwjdpfsykkivsx Al Iel • Never used in production • Inventory stock from project surplus • Absolutely clean interior • No corrosion • No signs of use • As-new industrial condition • Immediately available Suitable for • Wash solutions in pharmaceutical processes • WFI / PW applications • CIP media • Buffer and process solutions • Biotechnology • GMP production systems • Sterile liquid processes Documentation – fully available and structured Comprehensive, project-specific quality and manufacturing documentation included, such as: • EU declaration of conformity and warranties • Reports and EU component verifications • Assembly documents • Component drawings • TÜV certificate with acceptance report • Nameplate documentation • TÜV design review and certification • Welder lists, welding procedure qualifications, samples • Analysis certificates for welding filler material • Analysis certificates for shielding gas • Manufacturer qualification certificate • Non-destructive testing (NDT) reports • Material certificates (3.1) • Calibration certificates • Internal pressure test report • Dimensional accuracy check • Surface roughness report • Surface treatment report • Operating and maintenance manuals (unit) • Operating and maintenance manuals (components) • FAT documentation (Factory Acceptance Test) Complete documentation package available digitally. Special Feature This is not a standard tank, but a premium, custom-built unit in genuine pharmaceutical quality with certified pressure design, documented manufacture, and full PED compliance including TÜV acceptance. The heavy-duty construction, large connections, and CIP integration make this vessel ideal for demanding GMP applications.