Used Gmp Qtopic380 for sale (122)

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. Dkodpfx Aoyl H Svep Dju 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. 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, Year of construction: 2020, functionality: fully functional, tank capacity: 9,000 l, Equipment: documentation/manual, BRINOX 9000 L GMP Wash and Elution Solution Tank Horizontal Stainless Steel Pressure Vessel – Year of Manufacture 2020 – Complete FAT & GMP Documentation BH6752-BH1001 Package 32 Manufacturer: BRINOX Process Systems Serial Number: 1003558 Year of Manufacture: 2020 Nominal Volume: 9,000 liters Design: GMP-compliant stainless steel pressure vessel Application The tank was used in a pharmaceutical manufacturing facility. Suitable for preparation, storage, and dispensing of process solutions in GMP environments. Construction and Equipment - Cylindrical stainless steel tank in horizontal configuration - Front-end process connections - Large manway with pressure lock - Integrated CIP (Cleaning-In-Place) system with spray ball - Highly polished internal surfaces - Hygienic product-contact connections - Multiple instrumentation and sensor nozzles - Documented weld seams with full traceability - Separate stainless steel support legs included Dkodpfoykkk Hox Ap Dju Condition Visually and technically in very good condition. Internal surfaces are mirror-polished and clean. No visible damage to the shell or connections. Accessories and attachments present as per photo documentation. FAT and Documentation Status According to FAT documentation “IT-11.1 Inspection of Welding Documentation”, weld documentation was inspected during the Factory Acceptance Test (FAT 01, 23.10.2020). The following were confirmed, among others: - Identification of welders and weld inspectors - Welder qualifications according to EN ISO 9606-1 - WPS and WPQR documentation - Proof of shielding gas suitability - Documented test welds - Visual spot checks with no findings - Traceability according to material certificates 3.1 The complete weld documentation is part of the Turn-Over-Package. Documentation – Fully Available - FAT plan and FAT report - Layout and construction drawings - P&ID diagrams - Calibration protocols - Surface finish and roughness tests - Leak test - Welding plan - WPQR - WPS - Welder qualifications - Borescope inspection report - Incoming goods inspection reports - Sensor calibrations The complete technical documentation is available digitally. Special Features - Fully documented GMP configuration with certified welding documentation and extensive quality package - Ideally suited for reinstallation in pharmaceutical plants or environments requiring validated applications.

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 Dkodeylnppepfx Ap Dsu • 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 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.

Year of construction: 2020, condition: new, functionality: fully functional, Manufacturer BRINOX Machine designation CIP System CS6720 Model LEP12 – CIP module with insulated buffer tank, 200 L Year of manufacture 2020 Condition New, unused, originally packaged, never installed, never commissioned System type Modular CIP system (Cleaning in Place) on stainless steel frame, fully pre-assembled. Comprising insulated CIP buffer tank, centrifugal pump, heat exchanger, stainless steel piping module, valve technology, measuring and control equipment, as well as media connections. Dsdpfxjyl H Hts Ap Dsku Frame dimensions Approx. 2330 x 1224 x 2127 mm Buffer tank Working volume: 200 liters Total volume: 278 liters Cylindrical design with dished ends according to DIN 28011 Operating pressure: -1 to +3 bar Test pressure: 5.4 bar Permissible temperature: -10 °C to +150 °C Operating temperature: 0 °C to +85 °C Fluid group: 1 Insulation: Glass wool with low chloride content (

Condition: new, Year of construction: 2020, functionality: fully functional, Equipment: documentation/manual, Machine Description BRINOX LEP 12 – CIP System Precipitation PRE LEP 12 CS6725 Package 5 Manufacturer BRINOX Prozess- und Edelstahltechnik GmbH, Offenburg Year of Manufacture 2020 Serial Number 1003614 Dodpfx Asyl H Taop Deku Technical Data Compact CIP skid system in stainless steel frame design. Product designation: LEP 12 – CIP System Precipitation PRE. Dimensions approx. 1520 x 970 x 1994 mm. Product-contact parts: Stainless steel 1.4435. Frame and structural components: Stainless steel 1.4301. Integrated shell-and-tube heat exchanger by NEUMO. Centrifugal pump in hygienic design. Piping fully welded in pharmaceutical grade. Insulated media lines. Fittings incl. GEMÜ ball valves. Various integrated pressure gauges and measuring instruments. Calibrated pressure measurement system (Fluke pressure transducer, measuring range −1 to 20 bar, resolution 0.001 bar, accuracy 0.06 % FS). Media Connections: NaOH Acetic acid CIP supply CIP return Black steam Black steam condensate Neutralized wastewater Pressure tightness test performed with compressed air. Test pressure range approx. 3.19–3.24 bar. Maximum measured pressure drop < 0.015 bar during the test period. Result: passed. Application CIP cleaning system for pharmaceutical process plants, especially for precipitation vessels. Suitable for caustic and acid cleaning as well as steam integration. Designed for hygienic applications in pharmaceutical production. Construction Welded, compact skid design with robust stainless-steel frame construction. Hygienic piping layout with defined media paths. Integrated shell-and-tube heat exchanger for CIP media temperature control. Integrated process pump, valve technology, and instrumentation on a compact frame. General tolerances according to EN ISO 13920. Industrial design with crane lugs for transport. Condition New, unused, and in original packaging. The system was only inspected as part of the FAT process and has never been in production use. FAT / Documentation Status Complete Factory Acceptance Tests carried out. Pressure tightness tests successfully passed. Calibration certificates available. All test protocols fully documented. Complete Documentation List FAT documentation Pressure test protocols Calibration certificates P&ID 3D drawings Material and welding documentation Nameplate and manufacturer documentation Special Features Pharma-grade material selection. Compact, immediately ready-to-use skid unit. High-quality components from renowned manufacturers. Complete technical documentation available. Immediately available.

Condition: new, Year of construction: 2020, functionality: fully functional, Equipment: documentation/manual, Manufacturer: BRINOX Type: LEP2.3 – Wash Solution Temperature Control Unit Year of Manufacture: 2020 Serial Number: 1003507 LEP2.3 KK6761 Package 8 Tag No.: MR-INH-VPR61-KK6761 Equipment No.: 20023781 Technical Data System Type: Temperature control unit / heating and cooling module for wash solution (CIP or process washing system) Design: Compact, fully pre-assembled skid unit in robust stainless steel frame construction, crane-liftable via integrated lifting points. Frame and Construction: Welded stainless steel construction in industrial design, free-standing, multi-level piping configuration for optimal space utilization. Maintenance-friendly access from multiple sides. Integrated cable trays. Piping: Stainless steel process piping in hygienic design, welded and partially flanged. Multilayer thermal insulation of main lines and apparatus. Integrated drain and vent fittings. Valve Technology: Multiple manual ball valves (GEMÜ) in main and bypass circuits. Pneumatically actuated control and shut-off valves for automatic temperature regulation. Diaphragm and control valves integrated in the heating and cooling circuit. Instrumentation and Control: Temperature measurement points in both supply and return lines. Pressure sensors in the process section. Integrated flow measurement. Electrical junction box with protective labeling. Automatic temperature control via pneumatic control valve. Heat Exchanger: Cylindrical stainless steel heat exchanger, insulated and integrated into the piping system. Designed for controlled heating and/or cooling of the wash solution in a closed loop. Pump Technology: Two electrically driven centrifugal pumps with red-painted motors for process recirculation within the temperature control unit. Electrical: Electrical junction box with warning markings. Wired sensors and actuators. Prepared for integration into a central PLC or process control system. Application This system is used for precise temperature regulation of a wash solution within a pharmaceutical or biotechnological process system. Typical areas of application include CIP systems, production plant washing stations, and temperature-controlled cleaning processes in the pharmaceutical and biotechnology sectors. The wash solution circulates in a closed loop via pumps, is temperature controlled by the integrated heat exchanger, and continuously monitored by sensors. Temperature is regulated automatically via pneumatic control valves to maintain defined setpoints accurately. Construction Compact modular skid design with fully insulated main lines. Stainless steel surfaces in hygienic industrial finish. Clearly organized media routing and structured piping layout. Crane-transportable via integrated lifting points. Condition Year of manufacture 2020. Very good visual and technical condition. Professional execution in pharmaceutical plant engineering. Dodpfxsyl It Io Ap Doku FAT / Documentation Typically supplied with CE conformity, Factory Acceptance Test (FAT), and technical documentation including P&ID diagrams and material certificates for product-contacting components. Special Features Fully insulated temperature control module in a compact, high power density design. High-quality valve technology (GEMÜ). Multiple integrated measurement and control points. Suitable for validated pharmaceutical processes. Industrial, pre-assembled skid solution with clearly structured media routing.

Condition: new, Year of construction: 2020, functionality: fully functional, Equipment: documentation/manual, Manufacturer: BRINOX Type: LEP 2.3 – Washing Solution Temperature Control Unit Year of Manufacture: 2020 Serial Number: 1003561 Tag No.: MR-INH-VPR61-KK6751 Equipment No.: 20022779 Location: Germany Condition: New, unused, original packaging Technical Data System Type: Washing Solution Temperature Control Unit (Temperature Control Skid) Design: Compact, pre-assembled skid unit in stainless steel frame Frame Material: Stainless steel Insulation: Completely insulated piping and components Pumps: Two circulation pumps with electric motors Stainless steel pump housing Inline design Heat Exchanger: Integrated stainless steel heat exchanger Shell and tube or jacketed tube design Valves: Multiple GEMÜ ball valves Stainless steel valves Pneumatic control valves Safety valves Instrumentation: Pressure transmitter Pressure gauges Temperature measuring points Integrated flow measurement Electrical: Integrated control cabinet or terminal box Ready-wired for connection Industrial standard components Piping: Stainless steel process pipelines Fully insulated Flange and clamp connections Transport: Forklift- and crane-compatible Heavy-duty stainless steel base frame Application The temperature control unit is designed for controlled temperature regulation of a washing solution in pharmaceutical or chemical processes. Suitable for CIP and washing processes, pharmaceutical production lines, chemical processing plants, as well as temperature-controlled media circuits. Construction Compact, modular skid design Pre-assembled and ready to connect High-quality stainless steel construction Industrial-grade quality components, including GEMÜ valves Service-friendly design Condition New system Never used Original packaging Direct from manufacturer’s project Immediately available FAT and Documentation Status Technical documentation available Project documentation available Drawings available P&ID available Component lists available Operating manual available Special Features Dkodpoyl Ib Esfx Ap Dou Completely insulated process piping High-quality stainless steel construction Premium industrial components Ideal for new projects or as a replacement/redundant unit Immediate integration possible

Condition: new, Year of construction: 2020, functionality: fully functional, Manufacturer BRINOX Model LEP 12 – CIP System Precipitation PRE LEP 12 CS6721 Package 3 Year of manufacture 2020 Condition New, original packaging, unused. The system was tested exclusively at the factory as part of FAT. No commissioning, no production, no media contact during operation. Description Modular CIP process system for pharmaceutical applications in hygienic stainless steel design. Compact skid-mounted unit with fully integrated measuring, pump, and valve technology. Dimensions approx. 1520 x 970 x 1994 mm Materials Product-contact parts: Stainless steel 1.4435 Frame/Structure: 1.4301 Welding as per EN ISO 13920 Features – Shell-and-tube heat exchanger – Hygienic centrifugal pump – Magnetic-inductive flow meter – Conductivity measurement – Pressure transmitter – Temperature measurement points – Pneumatic seat and diaphragm valves – Stainless steel frame construction – CIP supply / CIP return – Media connections for NaOH, acetic acid, steam, condensate, wastewater Testing Comprehensive FAT performed including: – Layout check – P&ID review – Accessibility check for maintenance and calibration – Documentation review – Surface roughness test – Sensor calibration – Welding documentation review – Leak test with compressed air – passed Calibration certificates available. Material certificates 3.1 available. Complete welding documentation (WPS, WPQR, welder certificates, NDT evidence). CE-compliant execution. Scope of delivery Complete pre-assembled process module including documentation. FAT reports, welding records, material certificates, calibration certificates fully included. Dedpfsyl H H Tjx Ap Doku

Condition: used, Year of construction: 2004, Manufacturer: Gerteis Model: GMP-Polygran Macro Pactor 250/100/3 Year: 2004 Type: roller compactor, granulation unit for the pharmaceutical industry. Feeding screw: 0.1–180 rpm Compaction screw: 1–460 rpm Compaction zone with pressure rollers: 1–30 rpm Granulation zone with star rotor and screen: 0–180 rpm Force: 1 – 20 KN/cm Gap width: 1.0 – 6.0 mm Pressure roller speed: 1 – 30 rpm Roller diameter: 250 mm Roller width: 100 mm Capacity: 60 – 400 Kg/H (normal value: 200 Kg/h) Equipment dismantled and stored. Full electrical and technical file + program backup available. Dsdjx R Ar Rspfx Ap Deku Electrical, control, and safety cabinets are not available. These items can be quoted separately.

Condition: excellent (used), Year of construction: 2019, functionality: fully functional, 10 m2 workspace, 4 m2 dressing area 16 x Filter Fan Units Dodpfx Apezgcy Do Dsku Dimensions: Length: 6,000 mm Width: 3,000 mm Clear height: 3,600 mm (adjustable depending on ceiling and installation space) Area: 14 m² Brecon BCPS cassette system: Panel thickness: 70 mm Maximum wall height: 6 meters Standard panel width: 1,200 mm Aluminum frame profiles Finish: 0.6 mm coated steel or 3 mm HPL (RAL 9010) Flush-finished seams with cleanroom sealant. Ceiling Brecon BCPS system ceiling: Panel thickness: 50 mm Walkable ceiling option Load-bearing capacity up to 150 kg/m² Suitable for integration of: HEPA filter units (FFU) LED cleanroom lighting Air diffusers Utilities (data, electrical, gases) Chemically resistant ETP rubber Flat, cleanable design Optional with access control or interlock. Air handling Depending on desired classification: ISO 8 (production, assembly, packaging) ISO 7 (pharmaceutical, medical devices, precision engineering) GMP C/D possible, depending on the installation concept. Indicative bill of materials Component Specification Walls BCPS 70 mm panels Ceiling BCPS 50 mm system ceiling Doors 1–2 cleanroom doors Height 3,600 mm, adjustable in height

Condition: used, Pneumatic pick and place manipulator, loading unit similar to a SCARA robot with a parallel gripper. Handling device, handling system, pick-up gripper, loading gripper for automation. Horizontal axis with guide cylinder, linear module type SM 32/150 (column module GEMOTEC). Vertical axis with guide cylinder, linear module type SM 20/060 (column module GEMOTEC). Parallel gripper type GMP 20. Load capacity: max. 2 kg. Horizontal movement: 150 mm (pneumatic). Vertical movement: 60 mm (pneumatic). Vertical adjustment on the two support columns: 435 mm (manual, with clamping). Support columns, vertical guide column: Ø 45 mm. Guide column, linear module type SM 32/150: Ø 20 mm. Guide column, linear module type SM 20/060: Ø 12 mm. Mounting foot: 180 x 75 mm. - Can be moved pneumatically in two axes. - Part gripper, parallel gripper type GMP 20 (65 x 35 mm). Space requirement L x W x H: 550 x 160 x 550 mm. Weight: 17 kg. Very good condition. Dksdpfx Aez D Hxisp Deu Various manipulators available, see our webshop.

Condition: good (used), Used Comi Cóndor HX / GMP 316L stainless steel Atex-rated horizontal centrifugal peeler. The unit features a perforated basket with a diameter of 1150mm. Maximum load 280kg, maximum cake capacity 222 litres. Internal design pressure rated at +0.5/-0.5 bar at 50°C. The unit is equipped with main drive, hydraulic powerpack, mounting springs and two control cabinets. Material: Stainless steel 316/316L Technical features Model: HX/GMP Maximum load (density 1.25 kg/dm³): 280 kg Condition: As is Manufactured by: COMI-CONDOR Dkodpfxjynb Nuo Ap Dsu

Condition: new, Year of construction: 2020, functionality: fully functional, BOSCH Pharmatec CIP System 8X0400 – Never Used – GMP Pharma Version For sale is a complete BOSCH Pharmatec CIP (Cleaning in Place) system in new condition (Never Used). The system was manufactured in 2019/2020 but was never put into operation. Since delivery, it has been stored professionally and is in excellent condition. The system was developed according to the highest GMP standards and is ideally suited for the pharmaceutical, biotechnology, vaccine, and food industries. Technical Data Dsdpfx Apszpy Nzo Djku Manufacturer: Bosch Pharmatec GmbH (now Syntegon) Type: CIP Unit 8X0400 Year of Construction: 2019 / 2020 Condition: Never Used / New GMP Version Stainless Steel Design CE Marking Immediately available Scope of Supply BOSCH Pharmatec CIP Unit 8X0400 Stainless Steel Water Tanks CIP Satellites Complete Pump Skids KPA Hygienic Pumps Endress+Hauser Measuring and Control Technology Hygienic Stainless Steel Piping Valves and Fittings Heat Exchangers Original Bosch Documentation P&ID Flow Diagrams Layout Drawings and Technical Documents Important Note The system is offered without pneumatic components and without control (automation). This allows the system to be individually adapted to the buyer's requirements and equipped with a modern PLC, pneumatic, and automation solution as desired. This offers maximum flexibility for new installations or integration into existing production facilities. Application Areas Pharmaceutical Industry Biotechnology Vaccine Production Sterile Production Facilities API Manufacturing Supply of Purified Media GMP Production Plants Contract Manufacturing (CMO) Advantages Original Bosch Pharmatec Quality Never Put Into Operation High-Quality GMP Version Complete Technical Documentation Available Flexible Retrofitting of Control and Pneumatic Technology According to Customer Requirements Immediately Available Significantly Cheaper Than a Comparable New System The system can be inspected by appointment. We will gladly send you further photos, technical documents and drawings upon request.

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: Djdexxz T Hspfx Ap Doku 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: 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

Year of construction: 2018, condition: used, This listing is for a GE Healthcare UniFlux 120 Tangential Flow Filtration (TFF) System. 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) Dkedpexxx Inofx Ap Dou - Control System: UNICORN software (FDA 21 CFR Part 11 compliant)

Condition: ready for operation (used), functionality: fully functional, TECHNICAL DETAILS Sterilization process: Vacuum-assisted steam sterilization Sterilization temperature: 121–134 °C Vacuum cycles: Pre- and post-vacuum Chamber material: Stainless steel AISI 316L Pipe material: Stainless steel AISI 316L MACHINE DETAILS Control: PLC-based control Operation: HMI touchscreen Monitoring: Real-time cycle control with batch documentation Sensors: Integrated temperature and pressure sensors Standards: EN 285, PED, ISO 9001, GMP Validatability: According to ISO 17665 EQUIPMENT Stainless steel sterilization chamber with polished surface Vacuum pump system for pre- and post-vacuum Steam generation and steam distribution system PLC control with HMI touchscreen Integrated temperature and pressure sensors Diagnostics: Integrated self-test functions Media supply: Steam, water, compressed air, and power supply Door operation: Automatic Dodpoz I Ti Nsfx Ap Djku Door locking: Safety interlock to prevent opening under pressure

Condition: refurbished (used), Year of construction: 2013, functionality: fully functional, PAGO System L600 Pharmaceutical Labeling Machine | Extensively modernized | GMP | Immediately available Manufacturer: PAGO Etikettiersysteme GmbH (Fuji Seal) Model: System L600 Year of manufacture: 2013 For sale is a high-quality PAGO System L600 labeling machine for the pharmaceutical industry. The machine is suitable for labeling vials, injection bottles, and other cylindrical containers in a GMP environment. The machine was already upgraded and modernized at the factory in 2018 to handle additional product formats. In 2022, we purchased the machine used and immediately took it to the manufacturer, Fuji Seal / PAGO Germany. There, it was completely inspected, serviced, and extensively modernized. Investments of €60,200 were made in these measures. Before delivery, a complete Factory Acceptance Test (FAT) was carried out at the Fuji Seal factory. The machine is in very good technical condition and is ready for immediate use. Equipment Laetus/Keyence vision system for print and code inspection New Allen / Novexx thermal transfer printer Siemens PLC control Touchscreen operation Unwinding station Outfeed station Servo drives Stainless steel GMP design Complete protective enclosure Original documentation Technical data Output up to 120 products/min For vials and injection bottles GMP-compliant design Year of manufacture 2013 Manufacturer: PAGO Etikettiersysteme GmbH Why is the machine being sold? Dksdpfxozpzbfj Ap Deu For our new pharmaceutical CMO plant, we have purchased two new labeling machines. Due to space limitations, this machine is no longer needed. Advantages Extensive modernization by Fuji Seal / PAGO Documented investment of €60,200 Factory upgrade already in 2018 Complete FAT at the manufacturer Very well-maintained condition Immediately available Significantly cheaper than a new machine A comparable PAGO/Fuji Seal pharmaceutical labeling machine costs over €450,000 in 2026, depending on the equipment and automation. Inspection is possible at any time by appointment. We will gladly send you further photos, videos, and technical documentation upon request.

Condition: used, This listing is for the Envair Technology B102 Microbiological Safety Cabinet + Mobile Stand The unit is in full working condition and is ready for immediate use Overview: Envair Technology Bio 2 Essential (B102 Series) Certifications & Intended Use Fully compliant with BS EN 12469:2000, ensuring reliable biosafety standards. Envair Technology Suitable for handling biological agents up to ACDP Hazard Group 3, provided proper laboratory siting. Ideal for cell culture and related work. Envair Technology Design & Construction Width: 1200 mm. External body: Constructed from white polyester-coated mild steel. Work zone: Lined in 304-grade stainless steel with side-glazed panels. Work surface: Removable and dished, crafted from 316-grade stainless steel. Envair Technology Airflow & Filtration Offers recirculating or ducted configurations. Equipped with downflow HEPA filtration (Class H-14, ≥ 99.995% efficiency) according to EN 1822‑1 standards. Lighting & Fans Illuminated using low-energy LED lighting mounted external to the work area. Ventilation is powered by independent EC-type energy-efficient fans, both above and below the working zone. Envair Technology Control Interface Features an integrated positive-touch membrane control panel positioned above the work area, with animated display feedback. Envair Technology Compliance & Standards In addition to BS EN 12469:2000 and HEPA filter standards, the Bio 2 Essential cabinets also meet: Dedpfxoxhfpkj Ap Deku IEC 61010‑1:2010 Air quality standards: ISO Class 5 (BS EN ISO 14644‑1:2015) and EU GMP Grade A.

Condition: used, driver cabin: other, gearing type: other, Other: * Trade-in and purchase of vehicles and machines possible. * Sales price excluding transportation and transfer. Djdpfx Apozimd Ss Djku * No liability for printing & typing errors. * Errors, changes and prior sale reserved. * Offer subject to change. * Photos may differ. Price applies to existing condition. * All information without guarantee. - .

Condition: used, mileage: 1,63,000 km, power: 265 kW (360.30 HP), first registration: 10/2019, fuel type: diesel, overall weight: 26,000 kg, axle configuration: 3 axles, color: white, gearing type: automatic, emission class: euro6, Year of construction: 2019, Equipment: ABS, air conditioning, electronic stability program (ESP), * Mercedes-Benz Antos 2536 6x2 garbage truck * Euro 6d emission standard * Automatic transmission * Geesink body type: GMP IV 23H25, manufactured in 2019, approx. 23 m³ capacity * Steerable rear axle * Lift axle * Leaf spring/air suspension * Lane keeping assist Dksdpjzp Tpzofx Ap Dju * Air conditioning * 3-seater * Differential lock * Reversing camera * Heated seats * Radio/CD

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 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. Dedpoxv Dhbofx Ap Doku 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 the Cytiva AxiChrom 300/300 Chromotography collumn The unit is in full working condition and is ready for immediate use 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. Dkjdpfx Apjxhdwyj Deu 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, System Overview Djdpfxoxqq Dxo Ap Djku 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. - Designed for validation and GMP compliance (USP/EP WFI quality).

Condition: used, maximum load weight: 32,950 kg, overall weight: 39,000 kg, axle configuration: 3 axles, first registration: 02/2021, next inspection (TÜV): 03/2027, loading space volume: 49 m³, total length: 10,800 mm, total width: 2,555 mm, total height: 3,600 mm, Equipment: ABS, In accordance with our "General Terms and Conditions," without any guarantee or warranty, we can offer you the following vehicle today, subject to final sale, errors, typos, and prior sale: Reisch, approx. 49 cubic meter grain tipper (Vehicle 684) First registration: February 25, 2021 Approx. 49 cubic meter loading volume Permissible gross vehicle weight: 39,000 kg Unladen weight: 6,050 kg Payload: 32,950 kg Overall length: 10,800 mm x Overall width: 2,555 mm x Overall height: 3,600 mm Rollover tarp, platform Hinged tailgate with grain slide Clean floor and walls GMP certified Foldable underrun protection 2 x reversing lights 2 x 12-ton, 2-speed geared winch SAF disc 1st lift axle Tires: 385/65R22.5, 1st approx. 50/70%, 2nd approx. 80/70%, 3rd approx. 70/50% Semi-fender mudguards Access ladder over semi-fender mudguards Shovel and broom holder on the driver's side, front TÜV (technical inspection) valid until 03/2027, emissions test valid until 09/2027 Price: €23,000.00 (net) Djdpfez Iihzjx Ap Deku All information is provided without any guarantee or warranty. Our "General Terms and Conditions" apply. The place of jurisdiction for both parties for disputes up to €10,000 is the district court of Ludwigslust; for disputes exceeding this amount, it is the regional court of Schwerin. Subject to errors, typos, and prior sale.

Condition: used, This listing is for an ÄKTA ready™ Chromatography System The unit is in full working condition and is ready for immediate release Djdpfx Apeyitvps Deku The ÄKTA ready™ Chromatography System is a single‑use liquid chromatography platform engineered for bioprocessing, process scale‑up, and GMP‑regulated manufacturing of biologics, including monoclonal antibodies, recombinant proteins, viral vectors, nucleic acids, and other sensitive therapeutic products. Key Characteristics - Single‑use disposable flow paths — eliminate the need for cleaning and cleaning validation between runs, reduce downtime, and minimize cross‑contamination risk. - Flexible operation — available in multiple configurations (isocratic, gradient, variable UV, extended) to match different purification needs. - Scalable platform — flow kits for low and high flow rates support a wide range of process volumes; systems scale from small‑batch purification to larger process requirements when paired with larger ÄKTA ready™ XL models. - Designed for GMP environments — extensive documentation and regulatory support help meet compliance demands in regulated biopharmaceutical production