MPGL02GH2
Millipak® 20 Gamma Gold Capsule Media: Sterile Durapore® 0.22 µm
Chemistry: Hydrophilic Polyvinylidene Fluoride (PVDF) Inlet: 1/4 in. Hose Barb Outlet: 1/4 in. Hose Barb with Bell
Synonym(s):
Sterile Millipak-20 Filter Unit 0.22 μm 1/4 in. HB/HB w/bell, Durapore® 0.22 µm, Millipak® Capsule
Select a Size
About This Item
Product Name
Millipak® 20 Gamma Gold Capsule Media: Sterile Durapore® 0.22 µm, Chemistry: Hydrophilic Polyvinylidene Fluoride (PVDF) Inlet: 1/4 in. Hose Barb Outlet: 1/4 in. Hose Barb with Bell
Quality Segment
material
PVDF membrane, PVDF vent cap, polycarbonate , polycarbonate support
sterility
irradiated, sterile
product line
Millipak®
feature
hydrophilic
manufacturer/tradename
Millipak®
parameter
0.35 bar max. differential pressure (5 psid) at 123 °C (Forward), 0.7 bar max. differential pressure (10 psid) at 25 °C (Reverse), 1.5 L/min flow rate at 1.75 bar (ΔP), 1.7 bar max. differential pressure (25 psid) at 80 °C (Forward), 10 L process volume, 25 °C max. temp., 4.1 bar max. differential pressure (60 psid) at 25 °C (Forward), 5.2 bar max. inlet pressure (75 psi) at 25 °C
technique(s)
sterile filtration: suitable
filtration area
100 cm2
inlet connection diam.
1/4 in.
outlet connection diam.
1/4 in.
impurities
≤0.5 EU/mL (LAL test, Aqueous extraction), <0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
gravimetric extractables
≤1 mg/device
matrix
Durapore®
pore size
0.22 μm
bubble point
≥3450 mbar (50 psig), air with water at 23 °C
fitting
inlet hose barb, outlet hose barb (with bell), (6 mm (1/4 in.) Hose Barb Inlet and Outlet with filling bell)
shipped in
ambient
General description
Analysis Note
Other Notes
- Organism Retention: Microorganism
- Mode of Action: Filtration (size exclusion)
- Application: BioProcessing
- Intended Use: Reduction or removal of microorganism/bioburden
- Instructions for Use: Please refer Wetting Instructions for Filter Units with Durapore® Membrane user guide
- Storage Statement: Store in dry location
- Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations.
Legal Information
Still not finding the right product?
Explore all of our products under Millipak® 20 Gamma Gold Capsule Media: Sterile Durapore® 0.22 µm
Stay compliant with GMP using the Emprove® Program
Accelerate qualification, maintain compliance, and save time with Emprove® Dossiers.
Note: you will be brought to EmproveSuite.com. Your username and password are separate from SigmaAldrich.com and may differ.
Register for free and access Emprove® Dossiers within minutes. Upgrade your subscription plan to unlock advanced and customized content in the Emprove® Suite
Not finding what you are looking for? Visit the Emprove® Program Help page.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Articles
Key aspects of single-use assembly qualification including quality by design (QbD), quality risk management (QRM) and operator handling and training.
Before adoption of single-use technologies in biomanufacturing, manufacturers must assess the risk to the drug product from potential leachables. This article highlights a general approach based on the United States Pharmacopeia (USP).
Global Trade Item Number
| SKU | GTIN |
|---|---|
| MPGL02GH2 | 04053252571268 |