Used Uhlmann Usp for sale (191)

Year of construction: 2016, condition: like new (used), Anton Paar MCP 150 Polarimeter – Used, Excellent Condition This Anton Paar MCP 150 Polarimeter is offered in excellent condition from a well-maintained GMP-compliant laboratory. Ideal for laboratories requiring precise optical rotation measurements and full 21 CFR Part 11 compliance, especially in pharmaceutical, fragrance, and food quality control applications. Key Features: - Model: MCP 150 - Wavelength: 589 nm (LED) - Measuring range: ±89.9°, resolution 0.001°, accuracy ±0.01°, repeatability ±0.01° - Peltier temperature control (15–35 °C), with ±0.1 °C accuracy - Compact design: 370 × 320 × 130 mm, 8.6 kg - Interfaces: USB, Ethernet, RS232, CAN bus - Compliant with: 21 CFR Part 11, Ph. Eur., USP, JP, GAMP5, GMP Fsdpfxowbhkte Aa Njpg Included Accessories: - Quartz control plate (+8°Z, +3°OR) with Toolmaster™ wireless ID - 100 mm stainless steel polarimetry tube with Luer adapter and Peltier temperature control - USB dongle for Anton Paar PS software license - Full original documentation including: - Installation Qualification (IQ) - Calibration certificates - User manual (German) Condition: Used, but in excellent working condition. Device and accessories are clean, well-maintained, and fully functional. Directly from a controlled GMP environment Located in Liestal, Switzerland.
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Condition: new, Year of construction: 2020, functionality: fully functional, For sale: 3 × new Proxcys BCC600 chromatography systems (year of manufacture 2020, original packaging, CE certified) We are offering three unused, originally packaged Proxcys BCC600 batch chromatography columns from 2020. The units are brand new, fully CE-certified, and comply with GMP requirements for pharmaceutical and biotechnological applications. Technical data (per unit): • Manufacturer: Proxcys • Model: BCC600 • Year of manufacture: 2020 • Condition: New, in original packaging • CE marking: Yes • Operating pressure: 0.4 bar • Max. temperature: 30 °C Fpedpfjxyp Riox Aa Neg • Dimensions (L × W × H): 1810 × 2000 × 2350 mm • Weight: approx. 1,600 kg Construction & features: • High-quality chromatography column made of stainless steel 1.4435 (316L), electropolished (Ra ≤ 0.8 µm) • Acrylic column (PMMA, USP Class VI) with integrated 360° CIP spray system • Electromechanical lifting mechanism with 3 Siemens load cells • Three-blade paddle agitator with frequency converter • BioControl connections (DN15–DN65) for product, buffer, and safety applications • Safety valve, pressure gauge, sensors for pressure, level, and temperature • PLC control system with HMI, emergency stop, status lights, and acoustic signal module Special features: • New & in original packaging – never put into operation • GMP-compliant design • Ideal for protein purification, chromatography, downstream processing, and pharmaceutical production • Complete technical documentation included (Functional Specification, P&ID, Drawing, Electrical Schematic) Availability: 3 units Location: Germany Price: On request. The original new price in 2020 was €320,000 per unit; all three units together were €960,000.

Condition: excellent (used), Packo PHP 2 Pharmaceutical Process Pump The Packo EHEDG and 3A-certified PHP2 series pharmaceutical process pumps are used for the most demanding sterile applications in the pharmaceutical, biotechnology, and semiconductor industries. These perfectly cleanable pumps feature pump housings made of thick, cold-rolled 316L stainless steel, which are 100% non-porous and extremely smooth. The pumps feature fully machined, open impellers made of 1.4435 material. Thanks to their gap-free design and final electropolishing, the PHP2 series pumps are perfectly cleanable, making them a reliable component in your production process. Areas of Application These perfectly cleanable process pumps are the ideal solution for clean water circuits, cleaning applications, etc. Typical fluids include pure water, WFI, CIP, syrups, etc. Your Benefits High pump efficiency leads to lower energy consumption Low NPSH values: reduced risk of cavitation Electropolished: perfectly cleanable Simple design and maintenance: less downtime Standard components Fully certified (roughness value, FDA, USP, 3.1 for wetted parts, certificate of conformity, etc.) Suitable for SIP Robust construction according to ASME BPE guidelines Wetting parts < 0.4 µm Manufacturer: Packo Type: PHP 2/40-1857752 Flow: 14 m³/h Height: 59 m Weight: 91 kg Find more items - new and used - in our shop! International shipping costs on request! Fpodpfx Asw Hc Hmoa Nog

Condition: used, This listing is for 1 of 2 QuattroFlow QF15PTIU Single-use Pump Diaphragm Pump. The unit is in full working condition and is ready for immediate release. The QuattroFlow QF 150 PTIU is an advanced single-use quaternary diaphragm pump tailored for biopharmaceutical applications, offering several notable features and benefits that enhance its functionality in sensitive environments. Here’s a detailed look at its specifications and advantages: Key Features and Specifications: Flow Rate: Operates within a range of 0.02 to 3.2 lpm (0.01 to 0.85 gph), making it highly adaptable for various bioprocessing tasks. Design: Utilizes a 4-piston diaphragm positive displacement system, which ensures total product containment. This design minimizes the risk of abrasion and particle shedding, crucial for maintaining product purity. Materials: Constructed from disposable machined polypropylene, the pump is designed specifically for single-use applications, significantly reducing contamination risks. Control System: Equipped with an integrated controller, allowing for automated operation and precise control over pump functions, which enhances efficiency and consistency in processes. Certifications: Complies with USP Class VI and 3.1B standards, as well as CFR FDA regulations, ensuring it meets the stringent requirements for biopharmaceutical manufacturing. Applications: The QF 150 PTIU is versatile and suitable for various critical applications, such as: Filtration Systems: Ideal for use in Tangential Flow Filtration (TFF) setups, where it can efficiently process biological solutions. Chromatography Systems: Effectively manages the flow of reagents and samples during separation processes. Feeding Pumps: Provides reliable and consistent dosing in various bioprocessing applications. Virus Filtration: Plays a pivotal role in ensuring the safety of biopharmaceutical products by filtering out contaminants. Fodpjxxz Iwefx Aa Njpg Sterile Filtration: Maintains sterility in critical processing steps, essential for product integrity. Key Benefits: Total Product Containment: Ensures that no product is lost or contaminated during transfer, vital for high-value biopharmaceuticals. Low Pulsation and Low Shear Operation: These features preserve delicate biological materials and maintain their integrity throughout the pumping process. Variable Flow Rate: Allows for flexibility in operations, accommodating different process needs easily. Quiet Operation: Minimizes noise during operation, making it suitable for laboratory and clinical environments. CIP/SIP Capable: Facilitates easy cleaning and sterilization, ensuring high hygiene standards are maintained. Autoclavable: Supports sterilization processes, enhancing its usability in critical applications. Single-Use Design: Reduces maintenance requirements and downtime, allowing for efficient workflow in biopharmaceutical settings.

Condition: used, This listing is for a Sartorius SECURA513-1CEU. The unit is in full working condition and is ready for immediate release. Integrated protection systems for minimizing your risk of obtaining incorrect results Real-time alarm messaging and interactive user guidance for levelling to prevent inaccurate results due to an unleveled balance Fpedpfoxzg Dvjx Aa Njg SQmin for automatic detection and active monitoring to ensure you are within the acceptable USP operating range for reliable results Fully automatic internal adjustment function, isoCAL, for the highest possible accuracy at all times Cal Audit Trail for easy, traceable documentation of all calibration and adjustment data Safe and clear documentation by sample and batch identifiers for keeping perfect track of weighing data GLP-|GMP-compliant printouts Standard password security features for protection against tampering and unauthorized access Integrated PC direct function and Plug & Work connectivity to a Sartorius printer

Condition: used, This listing is for a Sartorius Cubis MSE2202S-100-D0 Balance with printer. The unit is in full working condition and is ready for immediate release. The Sartorius MSE2202S-100-D0 is a top-of-the-line balance from Sartorius’ Cubis series, offering precision, advanced functionality, and robust design, making it ideal for various laboratory settings. With a significant capacity and a range of built-in applications, this balance is suited for demanding weighing tasks. Key Features: High Capacity and Readability: Capacity: 2,200g Readability: 10mg (0.01g) This allows for precise measurements of both small and larger samples, making it versatile for different applications. Generous Weighing Pan: Dimensions: 206 x 206mm (W x D) Ample space for weighing liquids, powders, pastes, or solid samples without risk of spillage. User-Friendly Control Panel: Features a keypad and LCD display with text prompts for easy navigation and activation of functions, enhancing user experience. Built-in Applications: Fodpfx Aexxzhdsa Nspg Comes with nine built-in applications for various tasks, including: Unit conversion isoCAL (automatic calibration) Density determination via the buoyancy method Net/total formulation Weighing in percent Counting Connectivity Options: Equipped with a USB port for data transfer to PCs (compatible with Windows 7, Vista, XP, 2000, ME, or 98SE) and an RS-232C port for connecting peripheral devices, allowing for easy integration into lab setups. Accuracy Features: isoCAL: Automatic internal calibration ensures precision based on temperature and time, reducing user intervention. Automatic Levelling: Achieved at the touch of a button, simplifying setup. Security Features: Includes a fastening point for attaching an anti-theft locking device, enhancing security in shared or public environments. Robust Design: Ingress Protection Rating: IP54, which protects against dust and water splashed from all directions, making it suitable for various lab environments. Operating Temperature Range: 5 to 40°C at 80% RH, ensuring reliable performance under different conditions. Technical Specifications: Capacity: 2,200g Readability: 10mg Linearity/Repeatability: 20mg/7mg Minimum Sample Weight (USP Standards): 10g Weighing Units: gram, kilogram, carat, pound, ounce, troy ounce, grain, pennyweight, milligram, parts per pound, Austrian carat, Newton, pound:ounce, microgram Display: LCD Power Supply: 100-240V, 50-60Hz (includes 120V line cord) Weighing Pan Material: Stainless steel Compliance: ISO, FDA, USP, GxP; IP54

Condition: used, This listing is for a Halo Labs Horizon Particle Analyzer The unit is in full working condition and is ready for immediate release (No PC/Monitor) The Horizon system from Halo Labs integrates Backgrounded Membrane Imaging (BMI) technology to accurately measure and characterize subvisible particles in a high-throughput, low-volume format. Originating from membrane microscopy, a USP lot release method, BMI images particles on a membrane surface. This fully automated, fluidics-free Horizon system employs disposable membrane plates and automated image processing for quick, reliable particle counts and sizing. Capable of characterizing particles in up to 96 samples per run using only 25 µL per sample, BMI is unaffected by solution refractive index, ensuring accurate measurement of translucent protein aggregates. Sophisticated image processing techniques are used to analyze and acquire particle data, beginning with a background image of the membrane. After filtering samples by vacuum and capturing particles, the membrane is re-imaged with sample particles on its surface. The sample image is meticulously aligned with the background and processed pixel by pixel to remove background texture, achieving high contrast for the particles. This imaging approach yields high reproducibility and minimizes interference from membrane texture or imperfections. Key Features: Backgrounded Membrane Imaging (BMI) technology for precise particle measurement. High-throughput: Capable of analyzing up to 96 samples in a single run. Fodpfxexhgake Aa Nepg Low sample volume: Requires only 25 µL per sample. Fully automated, fluidics-free system for seamless operation. Accurate measurement of translucent protein aggregates, unaffected by solution refractive index. Sophisticated image processing for high reproducibility and minimal interference.

Year of construction: 2014, condition: used, This listing is for a Mueller PyroPure P4003 Pure Steam Condensing System. The unit is in full working condition and is ready for immediate release. This Unit was installed new in 2015 by Freestead Process Technology. This Unit is fitted with a Allen Bradley Compact Logix PLC and Panel View plus 1000 HMI's- Product Overview: The Mueller P4003 is a high-capacity pure steam condensing system, part of the trusted PyroPure series. Designed for pharmaceutical manufacturing, this system produces pyrogen-free and endotoxin-free water-for-injection (WFI) by condensing pure steam. Built to meet or exceed U.S. Pharmacopoeia (USP) standards for WFI, as well as CE marked and FDA compliant with 3.1B material certification. It is a versatile solution for facilities requiring both pure steam and WFI quality distillate. Its robust design and advanced features ensure reliable operation, compliance, and minimal maintenance. Key Specifications: Model Number: P4003 Capacity: 100 gallons per hour or 379 litres per hour of WFI-quality distillate. Pure Steam Inlet: 807 pounds per hour or 366 kilograms per hour. Coolant Requirement: 978 gallons per hour or 3702 litres per hour. Pure Steam Output Compliance: Pyrogen-free and endotoxin-free, meeting USP WFI standards. Core Features High-Quality Output: Produces pyrogen-free steam and WFI-quality distillate, ideal for pharmaceutical-grade applications. Utilizes a tangential nozzle design for optimal impurity separation in the pure steam generator. Efficient Design: Fully drainable components eliminate contamination risks and ensure clean operation. Electro-polished 316/316L stainless steel with a maximum surface roughness of 20 Ra for all product contact areas. USP Class VI-certified elastomers for enhanced safety and regulatory compliance. Ease of Maintenance: Removable tube bundle in the condenser allows for easy cleaning and inspection of critical surfaces. Requires only 24 inches of clearance on all sides for service and maintenance. Minimal instrumentation with just one control loop simplifies operation and reduces potential downtime. Installation Flexibility: Can be integrated with a PyroPure pure steam generator for dual production of pure steam and WFI. Optional stand-alone design for remote installation at the point of use, adding versatility to your setup. Applications: Pharmaceutical Manufacturing: Sterile environments, autoclave processes, and critical cleaning procedures. Fpodpexv Agcofx Aa Nsg Biotechnology: Providing WFI for sensitive biological processes. Healthcare: Humidification and sterilization in clean rooms or hospital sterilization units.

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. Fpodpfx Aexqq Dxja Nog - 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).

Year of construction: 2025, condition: used, 5Kg Thermo Scientific™ Tryptone Soy Broth (Soybean Case in Digest Medium EP/USP/BP/JP) (Dehydrated) New in original packaging Dated for use by end January 2026 Representing a price reduction of around 80% from the manufacturers retail price list Soybean Casein Digest (SCD), also known as Soybean-Casein Digest Medium or Tryptic Soy Broth (TSB), is a general-purpose nutrient medium used for cultivating a wide range of microorganisms, including bacteria and fungi. It's especially valuable because it's rich in nutrients derived from enzymatic digests of soybean meal and casein (milk protein) Used By 1. Pharmaceutical Industry - Sterility testing of pharmaceutical products (especially injectables and ophthalmic solutions). - Microbial limit testing of raw materials, finished products, and water. - Environmental monitoring (e.g., surface swabs, air sampling). Fpodpfx Aaoxv Azgo Neg 2. Medical Device Manufacturers - Used for sterility testing of surgical instruments, implants, catheters, etc. 3. Hospitals & Clinical Laboratories - For culturing bacteria and fungi from clinical specimens. - Used in blood culture bottles to detect septicemia. 4. Food and Beverage Industry - To test for microbial contamination in food products. - Used for hygiene monitoring in food processing environments. 5. Biotechnology and Research Laboratories - General purpose medium for growing a variety of microbes in research. - Useful in antibiotic sensitivity testing or microbiome studies. 6. Cosmetic Industry - For microbial limit testing and product safety validation.

Condition: used, This listing is for 1 of 2 GE Healthcare ÄKTAprocess Liquid Chromatography System. The unit is in full working condition and is ready for immediate release. The GE Healthcare ÄKTAprocess is a fully automated liquid chromatography system designed for process scale-up and large-scale biopharmaceutical manufacturing. With extensive configuration possibilities, it seamlessly transitions processes from small-scale ÄKTAexplorer and ÄKTApilot systems to industrial production. Featuring UNICORN control software, regulatory compliance, and high-performance liquid handling, the ÄKTAprocess is an essential tool for biopharmaceutical production. Key Features: Advanced Automation & Control: Automated Liquid Chromatography System: Ensures precise and reproducible separations. UNICORN Control Software: Provides intuitive process control and monitoring. Post-Purchase Configuration Options: Enhances usability and extends system lifespan. Scalability & Flexibility: Designed for Large-Scale Biomanufacturing: Supports seamless scale-up from lab to production. Customizable Configuration: Thousands of setup possibilities for different applications. Three Flow Rate Ranges: Handles up to 1,800 L/h, enabling high-volume production. Quality & Compliance: Built with USP Class VI Materials: Traceable, regulatory-compliant construction. Intelligent AxiChrom Column Packing: Ensures optimal separation performance. Full Regulatory Documentation & Services: Supports cGMP compliance. Compact & User-Friendly Design: Integrated Computer: Reduces footprint and minimizes plant clutter. Robust & Reliable Construction: Engineered for long-term operation in industrial settings. Specifications: Weight 450 kg (990 lbs) Dimensions (cm) 41L × 33W × 64H Dimensions (in) 16L × 13W × 25H Fodpfx Aoxxycgsa Nepg Benefits: Optimized for Bioprocess Scale-Up: Seamlessly transition from small-scale systems. Regulatory Compliance: Supports cGMP requirements with complete documentation. Highly Configurable: Adaptable to diverse biomanufacturing needs. Space-Efficient Design: Built-in computer minimizes workspace requirements. Applications: The ÄKTAprocess is ideal for biopharmaceutical production, including: Monoclonal Antibody Purification Vaccine Production Recombinant Protein Purification Gene Therapy & Cell Therapy Processing

Condition: used, This listing is for the Cytiva AxiChrom 300/300 Chromotography collumn Fpjdoxhdwyjpfx Aa Nsg 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. 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 GE Healthcare (now Cytiva) GE Axicrom 50/300 Chromatography column The unit is in full working condition and is ready for immediate use The AxiChrom line is a series of chromatography columns by GE Healthcare (now Cytiva), designed for preparative / process chromatography scale. The “50/300” refers to the diameter and tube length / “bed height” configuration. Key details: Fpsdpfx Aajxhdxds Neg 50/300: This is the smallest of the larger-scale columns. The “50” refers to the internal diameter (ID) of the column tube (50 mm), and “300” refers to the bed height (300 mm) for the “short” version. There is also a “50/500” for longer bed heights (500 mm). It uses axial compression, meaning the packing medium is compressed hydraulically from the top adapter, which helps ensure uniform packing density. The materials are designed to meet regulatory standards (USP Class VI, etc.

Year of construction: 2014, condition: used, This listing is for 1 of 2 Mueller PyroPure P7310 Pure Steam Generator. The unit is in full working condition and is ready for immediate release. This Unit was installed new in 2015 by Freestead Process Technology. The “Turned on Time”of the unit is 65,000 hours, but as this unit is 1 of 2 generators in an alternating system it does not indicate the "Steam Production Time". The sites steam requirements were low therefore the unit is in immaculate condition. They have full maintenance records backed up on their electronic technical system supplied as an extra by Freestead. This Unit is fitted with a Allen Bradley Compact Logix PLC and Panel View plus 1000 HMI's The Unit is supplied with- ⦁ Feed water pump system ⦁ Pure steam condensate sampling system ⦁ Pure steam analyser ⦁ Stainless steel sheathing and frame ⦁ Feed water analyser ⦁ Degasser The Mueller PyroPure P7310 Pure Steam Generator is a high-performance system designed to produce pyrogen-free pure steam suitable for the most demanding applications, such as pharmaceutical production, biotechnology processes, and healthcare sterilization. Built to meet or exceed U.S. Pharmacopoeia (USP) standards, the P7310 combines precision engineering, advanced technology, and robust materials to ensure consistent performance and reliability. They are CE marked and compliant with 3.1B material certification. The terms pure steam and clean steam are often used interchangeably in the pharmaceutical industry. However, not all equipment marketed as clean steam generators are up to the task of producing WFI quality pharmaceutical pure steam. Mueller pure steam generators use a tangential nozzle to provide separation of impurities from incoming feed water, producing pyrogen-free steam that, when condensed, meets USP requirements for water for injection. Key Benefits Superior Steam Quality: Produces pyrogen-free steam that meets USP requirements, ensuring safety and regulatory compliance. Optimized for critical applications like autoclaves, clean room humidification, and steam-in-place (SIP) sterilization. Achieves a 5 Log reduction in contaminants, which corresponds to a 99.999% reduction in microbial populations. This level of reduction ensures the highest degree of sterilization, making it ideal for pharmaceutical and biotechnology applications where absolute purity is critical. Efficient Design: External evaporator allows easy access for inspection and maintenance, reducing downtime. Fpodpfx Aajxv Af Sj Nog Separation column has no internal components requiring maintenance, eliminating potential for bacterial growth. Efficient heat transfer with a double-tube sheet evaporator minimizes stress cracking and maximizes performance. Ease of Maintenance: All critical components can be serviced with only 24" of clearance around the system. Fully drainable design prevents standing water, reducing contamination risks. Polished 316/316L stainless steel construction ensures durability and easy cleaning. Enhanced Operational Features: Minimal instrumentation is required, reducing complexity and operational costs. Simplified control with an Allen-Bradley PLC system, compatible with Ethernet for integration with facility systems. Certified elastomers (USP Class VI) provide enhanced compatibility with feed water and product. Specifications Performance: Pure Steam Capacity: from 0 to 700 kg/hr at optimal feed water conditions. Operating Pressure Range: Pure steam output pressure up to 50 psig. Mater...

Condition: used, This listing is for a Sartorius 36201S Balance 100G-15000G The unit is in full working condition and is ready for immediate release. Because of the large capacity (36 kg) but still good readability (0.1 g), this balance is need to be weighed, yet you still need granularity at the 0.1 g level. Examples: bulk materials in labs, industrial weighing in R&D, weighing heavy vessels/totes, formulation where fairly fine resolution is required. Not suitable for ultra-micro weighing (µg or mg) — it’s not an “analytical balance” in that sense, but rather a high‐capacity precision/industrial balance Maximum weighing capacity: 36,200 g (i.e., 36.2 kg) according to the data sheet for model “36201S”. Readability (i.e., smallest displayed increment): 0.1 g (100 mg). Weighing pan size: 400 mm × 300 mm (width × depth) for the high-capacity models. Fodpfxoxv Svte Aa Njpg Repeatability (typical deviation) < ±100 mg for this model. Linearity deviation < ±200 mg. Off-centre loading (eccentricity) specification: 300 mg at test load of 10,000 g. According to one listing the version “MCE36201S0-S00” is described as 36.2 kg capacity, 0.1 g readability, external calibration. According to another listing: “Maximum capacity 36200g – Readability 100mg – Weighing surface 400×300mm – Stainless steel” for version MCA36201S-2S00-O. Minimum weight (optimal) is noted as ~82 g (under USP 41 guidance: “820 d” rule) for this model class

Condition: used, This listing is for a Pall Allegro 200 L Single‑Use Mixer System. The unit is in full working condition and is ready for immediate release. The Pall Allegro 200 L single‑use mixer (model LGRMXTTE200L230B) is engineered for scalable, robust mixing in biopharmaceutical operations. It is part of Pall’s Allegro single‑use technology portfolio and is designed for applications from media and buffer preparation through final formulation. Built with proven engineering principles and compatibility with Pall’s Allegro biocontainer film formats, it offers ease-of-use, reproducible performance, and minimal validation burden. Key Features 4‑Pitch Blade Impeller – Effective, low-shear mixing over a broad range of conditions. Bidirectional Flow Capability – Able to run clockwise (up‑flow) or counterclockwise (down‑flow), accommodating different density fluids and solids. Bag Inflation System – Mixer bag inflation provides a controlled mixing envelope, allowing consistent performance across 50–200 L volumes, and supports gas blanketing. Flush Drain Valve – Helps avoid dead legs by removing settled materials that might otherwise be left unagitated. Retention of Allegro Film Materials – Uses the same film as standard Allegro 2D/3D biocontainers for material consistency, reducing requalification effort. Optional Baffle Kit – To mitigate air entrapment at higher rotational speeds for shear-sensitive processes. Technical Specifications Parameter Value Model / Part Number LGRMXTTE200L230B Operating Volume Range 50 – 200 L Voltage / Frequency 230 V AC, 50 Hz Current Draw ~5.1 A Motor Power 0.37 kW Rotation Speed Range 50 – 200 rpm Materials of Construction Mixer tote in 304 stainless steel; film, manifolds, ports in LDPE / PS / silicone etc. Weight (empty system) ~120 kg Footprint (W × D) 1,054 mm × 748 mm Height 1,378 mm Gas Supply Requirements 4 – 6 barg (for bag inflation / blanket) Operating Temperature Range 4 – 40 °C Fjdoxl Dxlopfx Aa Nepg Connections / Ports Inlet, gas inflation, exhaust, flush drain, powder addition ports etc. Applications Upstream Media Preparation – Efficient mixing of culture media and supplements. Downstream Buffer Preparation – Rapid homogenization of buffers or reagents. Final Formulation / Filling – Gentle mixing for drug products. Powder Addition / Reconstitution – Capable of handling solid-liquid mixing (e.g. powders) with repeatability. Shear-Sensitive Biologics – Low shear impeller design suitable for sensitive proteins or biologics. Benefits & Validation High Performance Mixing across Conditions – Demonstrated capability to mix a wide range of systems including liquid-liquid, solid-liquid, and viscous solutions with good speed and uniformity. Validated Materials & Safety – Components meet USP /, USP , , endotoxin limits, gamma-irradiation compatibility (up to 50 kGy), and leak-tested containers. Reduced Validation Overhead – Using the same film materials as existing Allegro biocontainers helps streamline requalification and process transfer. Minimal Dead Volume / Entrapment – Flush drain valve and optional baffles help prevent accumulation of settled solids. Scalable & Flexible – Supports operations from 50 L to 200 L with consistent mixing performance.