Skip to Content
MilliporeSigma

MCGL10S03

Millipore

Durapore® 0.22 µm, Millidisk® Cartridge

filtration area 500 cm2, hydrophilic

Sign Into View Organizational & Contract Pricing

Synonym(s):
Millidisk Cartridge 10-stack 0.22 μm Hydrophilic
UNSPSC Code:
23151806
eCl@ss:
32031690

material

PVDF
polysulfone
polysulfone support
silicone seal

Quality Level

sterility

non-sterile

sterilization compatibility

autoclavable compatible
steam-in-place compatible

product line

EMPROVE® Filter
Millidisk® 10

feature

hydrophilic

manufacturer/tradename

Millidisk®

parameter

0.35 bar max. differential pressure (5 psid) at 123 °C (Forward)
0.35 bar max. inlet pressure (5 psi) at 123 °C (Forward)
0.7 bar max. differential pressure (10 psid) at 25 °C (Reverse)
0.7 bar max. inlet pressure (10 psi) at 25 °C (Reverse)
1.7 bar max. differential pressure (25 psid) at 80 °C (Forward)
1.7 bar max. inlet pressure (25 psi) at 80 °C (Forward)
15 L/min flow rate at 3.5 bar (ΔP)
4.1 bar max. differential pressure (60 psid) at 25 °C (Forward)
4.1 bar max. inlet pressure (60 psi) at 25 °C (Forward)

technique(s)

sterile filtration: suitable

filtration area

500 cm2

impurities

≤0.5 EU/mL bacterial endotoxins (LAL test, Aqueous extraction)
<0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)

gravimetric extractables

≤2.5 mg/device

matrix

Durapore®

pore size

0.22 μm

input

sample type liquid

bubble point

≥3450 mbar (50 psig), air with water at 23 °C

cartridge code

not applicable

General description

Device Configuration: Cartridge
Stack Design: 10 Stak

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
5 SIP cycles of 60 min @ 135 °C; 5 autoclave cycles of 60 min @ 126 °C
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 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
Emprove is a registered trademark of Merck KGaA, Darmstadt, Germany
MILLIDISK 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