Skip to Content
Merck
CN
All Photos(1)

Documents

MPVL02GH2

Millipore

Durapore® 0.1 µm, Millipak® Capsule

Millipak® 20, sterile

Sign Into View Organizational & Contract Pricing
All Photos(1)
Synonym(s):
Sterile Millipak-20 Filter Unit 0.1 μm 1/4 in. HB/HB w/bell
UNSPSC Code:
23151806
eCl@ss:
32031690
NACRES:
NB.24

material

PVDF membrane
PVDF vent cap
polycarbonate
polycarbonate support

Quality Level

400

sterility

irradiated
sterile

product line

Millipak® 20

feature

hydrophilic

manufacturer/tradename

Millipak®

parameter

0.35 bar max. differential pressure (5 psid) at 123 °C (Forward)
0.7 L/min flow rate at 1.75 bar (ΔP)
0.7 bar max. differential pressure (10 psid) at 25 °C (Reverse)
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

0.1 μm

bubble point

≥4830 mbar (70 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

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Device Configuration: Gamma Gold Capsule

Packaging

Blister

Other Notes

These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
Directions for Use

  • 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.

Preparation Note

Sterilization Method
3 autoclave cycles of 90 min @ 123 °C; not in-line steam sterilizable
This product was manufactured with a Durapore® membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).

Analysis Note

Bacterial Retention
Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology.
Gravimetric Extractables: using sterilized device after a 200 mL flush and 24 hours in water at controlled room temperature
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥200 mL

Legal Information

ASTM is a registered trademark of American Society for Testing and Materials
Durapore is a registered trademark of Merck KGaA, Darmstadt, Germany
MILLIPAK is a registered trademark of Merck KGaA, Darmstadt, Germany

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service