Envair Safety Cabinet

Envair

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. Dodpfexhfpkox Aanjck 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: IEC 61010‑1:2010 Air quality standards: ISO Class 5 (BS EN ISO 14644‑1:2015) and EU GMP Grade A.

Condition: used, This listing is for a ENVAIR Safe Comfort Plus Safety Cabinet Dcjdpfxjxzgzzs Aanek

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 Dodpfexv Dhbex Aaneck 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. 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