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MPGL06CB1

Millipore

Durapore® 0.22 µm, Millipak® Capsule

sterile, filtration area 300 cm2, matrix Durapore®

Synonym(s):

Millipak-60 Filling Machine Filter Unit 0.22 m 1/4 in. NPT-1/4 in.HB

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About This Item

UNSPSC Code:
23151806
eCl@ss:
32031690
NACRES:
NB.24

Pricing and availability is not currently available.

material

PVDF membrane
PVDF vent cap
polycarbonate
polycarbonate support

Quality Level

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)
1.7 bar max. differential pressure (25 psid) at 80 °C (Forward)
30 L process volume
4.1 bar max. differential pressure (60 psid) at 25 °C (Forward)
5.2 bar max. inlet pressure (75 psi) at 25 °C
7.6 L/min flow rate at 2.9 bar (ΔP)

technique(s)

sterile filtration: suitable

filtration area

300 cm2

inlet connection diam.

1/4 in.

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This Item
MPGL06CL1MPGL06CF3MPSL06CL1
pore size

0.22 μm

pore size

0.22 μm

pore size

0.22 μm

pore size

5.0 μm pore size

technique(s)

sterile filtration: suitable

technique(s)

sterile filtration: suitable

technique(s)

sterile filtration: suitable

technique(s)

prefiltration: suitable

product line

Millipak®

product line

Millipak®

product line

EMPROVE® Filter

product line

Millipak® 60

filtration area

300 cm2

filtration area

300 cm2

filtration area

300 cm2

filtration area

300 cm2

manufacturer/tradename

Millipak®

manufacturer/tradename

Millipak®

manufacturer/tradename

Millipak®

manufacturer/tradename

Millipak®

sterility

irradiated, sterile

sterility

irradiated, sterile

sterility

irradiated, sterile

sterility

irradiated, sterile

General description

Device Configuration: Capsule
Number of stacked discs: 60 discs

Packaging

Double Easy-Open bag

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: after 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’.

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