Cellbag Bioreactor Chambers, Cytiva

Supplier: Cytiva

Certificates

Supplier: Cytiva

Certificates

About this item

Designed for use with WAVE Bioreactor systems, the Cellbag bioreactors are presterilized, single-use bags for noninvasive cell cultivation in research, development, and commercial manufacturing operations.

Presterile, single-use chambers
Fnon-invasive mixing of fluids using a WAVE Bioreactor instrument/system
Provides high mechanical strength and bio-inert fluid contact
Fluid contact layer is a USP Class VI ethylene vinyl acetate/low density polyethylene copolymer
Outer noncontact layer is made of low density polyethylene

Cellbag bioreactor components are similar to those used for biological storage bags and meet USP Class VI specifications for plastics. Validation data and Cellbag DMF are available to demonstrate biocompatibility.

Each Cellbag bioreactor has an air inlet and outlet filter, a needleless sampling port, an Oxywell2 dissolved oxygen probe insertion port, and a fill/harvest port. In addition, each Cellbag bioreactor can be customized with optional fittings such as ReadyMate aseptic connectors, dip tubes, an optical pH sensor embedded in the bag, screw cap ports, temperature ports, perfusion filters, and special tubing ports.

Certifications: USP Class VI. Testing is performed on irradiated film (50 kGy). USP XXII plastic class VI and ISO 10993 ISO 10993-4 Hemolysis study in vivo extraction method. ISO 10993-5 Cytotoxicity study using ISO elution method. ISO 10993-6 Muscle implantation study in rabbit. ISO 10993-10 Acute intracutaneous reactivity study in rabbit. ISO 10993-11 Acute systemic toxicity in mouse.

Ordering information: Validation is recommended for specific applications such as Monoclonal antibodies, Anchorage-dependent cells, Virus production, Vaccine production, Insect cell/baculovirus.

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• State issued document with your organization's Federal Tax ID Number
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• Any other ID issued by the State that includes the business name & address

* ATTN: California Customers may require additional documentation as part of the CA Health & Safety Code. Products that fall under this regulation will be placed on a mandatory 21-day hold after documentation is received. Avantor will not lift restrictions for residential shipping addresses.