NAU0020L30EP5
Mobius® Silver 2D Assembly End Ported Bag
20L Standard PureFlex™
Synonym(s):
Mobius®, Silver, 20 L Standard PureFlex™ End Ported Bag
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About This Item
material
PureFlex™ film (with hanger and support rod)
sterility
γ-irradiated (level of 25-40 kGY)
product line
EMPROVE® Single Use, Mobius®
packaging
package of 5 ×
parameter
20 L sample volume
technique(s)
buffer exchange: suitable, media fill: suitable
L
65.4 cm (25.7 in.)
W
43.1 cm (16.9 in.)
fitting
male Luer cap (Kynar), 1/4 in. female Luer connector (Luer Female 1/4"HB PVDF), 3/8 in. male connector (MPC Male 3/8"HB Polysulfone), female Luer outlet fitting (with cap), port (boat-ported 1/4" 3/8" 3/8"), female (MPC Female Polysulfone)
application(s)
cell therapy
gene therapy
life science and biopharma
liquid processing
mAb
ophthalmics
parenterals
pharma/biopharma processes
viral therapy
waste management
storage temp.
2-30°C
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General description
Mobius® Silver 2D assembly bags offer secure and sterile fluid handling solutions for biopharmaceutical applications. Each assembly includes a durable container, tubing with pinch clamps, and fittings. Available in volumes from 1L to 50L, these bags feature convenient hangers for easy lifting. Designed to enhance operational efficiency, our assemblies significantly reduce the risk of operator error and process disruptions.
Application
The Mobius® Silver 2D Assembly End Ported Bag is a versatile solution designed for the safe transfer and storage of sterile liquids, including cell culture media, buffers, and other solutions. Its robust design ensures minimal risk of contamination.
Features and Benefits
- Sterilized and ready to use
- User-friendly hanger design for convenient fluid management
- Mobius® Silver certificate of quality with every package
- Sterile disconnects with NovaSeal™ sealing technology
Other Notes
C-Flex 374 tubing, 3/8 in. ID x 5/8 in. OD, 18 in. long
Platinum-cured Silicone, 1/4 in. ID x 1/2 in. OD, 18 in. long
Pinch clamp
Legal Information
Certificates of Analysis (COA)
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Articles
This page provides an overview of USP <87>, <88>, and <1031>, compares bioreactivity testing, and describes the transition of our organization towards in vitro test methods.
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