About this item
The pure² Aseptic Isolator is an ideal solution for safe and efficient aseptic processing. Designed for a wide variety of critical aseptic processes, the pure² pairs the highest quality materials and technologies for unmatched protection of products and users.
Maintains unidirectional Grade A (ISO Class 5) conditions
- Smooth and easy to clean 316L stainless steel interior
- Selectable positive or negative pressure operation
- Large and fast airlocks to improve isolator productivity
- High performance nanox catalytic converters for short decontamination cycles
- Fully integrated, fast and safe H₂O₂ decontamination cycles with skanfog technology within each chamber
- HEPA filtered supply air (H14) and exhaust air (dual H14)
- DIN 12980 compliant for cytotoxic aseptic-toxic applications
The pure² Aseptic Isolator is a high-performance aseptic isolator designed for critical process applications requiring Grade A (ISO Class 5) conditions. This isolator ensures sterile, contamination-free handling through advanced HEPA filtration, H₂O₂ decontamination, and precise environmental control, making it ideal for applications that demand the highest level of product and user protection.
The pure² is engineered for aseptic processing, sterility testing, and contamination-sensitive workflows. It is commonly used in pharmaceutical applications where product protection is critical. With its modular design, customizable features, and fast decontamination cycles, the pure² isolator enhances productivity, flexibility, and operational efficiency, making it a superior choice for high-precision, contamination-controlled environments.
Available in 2 and 4 glove configurations, the modular space-saving design is flexible and customizable, with a diverse range of customizations and integrations such as pass-throughs and environmental monitoring.
IQ/OQ documentation package includes testing procedures and documentation for regulatory compliance. Onsite microbiological qualification H₂O₂ decontamination cycles with BIs, aeration confirmation, residual detection, and full reporting.