K002A05HH1

Opticap^® XL Capsule Filter

Name: Opticap<SUP>®</SUP> XL Capsule Filter
Brand: MM
Price: 294 EUR
Availability: InStock

pore size 0.2 μm, cartridge nominal length 5 in. (12.5 cm), filter diam. 4.2 in. (10.7 cm)

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1 PKG

€294.00

Estimated to ship on01 December 2025Details

About This Item

UNSPSC Code:

23151806

Key Documents

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material

polypropylene filter
polypropylene housing
polypropylene support
silicone seal

Quality Level

400

reg. compliance

meets FDA 21 CFR 177-182 (all component materials)

manufacturer/tradename

Opticap^®

parameter

max. inlet temp. at 25 °C
1.0 bar max. inlet pressure (15 psi) at 80 °C
2.75 bar max. inlet pressure (40 psi) at 60 °C
4.8 bar max. differential pressure (70 psid) at 20 °C
5.5 bar max. inlet pressure (80 psi) at 23 °C
80 psig max. inlet pressure

cartridge nominal length

5 in. (12.5 cm)

device size

5 in.

filter L

8.5 in. (21.6 cm)

filter diam.

4.2 in. (10.7 cm)

inlet connection diam.

9/16 in. , hose barb

inlet to outlet width

21.6 cm (8.5 in.)

impurities

≤0.25 EU/mL USP bacterial endotoxins (LAL test, aqueous extraction)

matrix

Clarigard^®

pore size

0.2 μm pore size

fitting

inlet/outlet connection for 14 mm (9/16 in.) hose barb

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This Item	K002A10HH1	K003A05FF1	K003A05TT1
Millipore K002A05HH1 Opticap^® XL Capsule Filter	Millipore K002A10HH1 Opticap^® XL Capsule Filter	Millipore K003A05FF1 Opticap^® XL Capsule Filter	Millipore K003A05TT1 Opticap^® XL Capsule Filter
fitting inlet/outlet connection for 14 mm (9/16 in.) hose barb	fitting inlet/outlet connection for 14 mm (9/16 in.) hose barb	fitting inlet/outlet connection for 19 mm (3/4 in.) sanitary flange	fitting inlet/outlet connection for 38 mm (1 1/2 in.) sanitary flange
material polypropylene filter, polypropylene support, polypropylene housing, silicone seal	material polypropylene filter, polypropylene housing, polypropylene support, silicone seal	material polypropylene filter, polypropylene housing, polypropylene support, silicone seal	material polypropylene filter, polypropylene housing, polypropylene support, silicone seal
impurities ≤0.25 EU/mL USP bacterial endotoxins (LAL test, aqueous extraction)	impurities ≤0.25 EU/mL USP bacterial endotoxins (LAL test, aqueous extraction)	impurities ≤0.25 EU/mL USP bacterial endotoxins (LAL test, aqueous extraction)	impurities ≤0.25 EU/mL USP bacterial endotoxins (LAL test, aqueous extraction)
parameter max. inlet temp. at 25 °C, 2.75 bar max. inlet pressure (40 psi) at 60 °C, 5.5 bar max. inlet pressure (80 psi) at 23 °C, 1.0 bar max. inlet pressure (15 psi) at 80 °C, 80 psig max. inlet pressure	parameter max. inlet temp. at 25 °C, 1.0 bar max. inlet pressure (15 psi) at 80 °C, 2.75 bar max. inlet pressure (40 psi) at 60 °C, 4.8 bar max. differential pressure (70 psid) at 20 °C, 5.5 bar max. inlet pressure (80 psi) at 23 °C, 80 psig max. inlet pressure	parameter max. inlet temp. at 25 °C, 1.0 bar max. inlet pressure (15 psi) at 80 °C, 2.75 bar max. inlet pressure (40 psi) at 60 °C, 4.8 bar max. differential pressure (70 psid) at 20 °C, 5.5 bar max. inlet pressure (80 psi) at 23 °C, 80 psig max. inlet pressure	parameter max. inlet temp. at 25 °C, 1.0 bar max. inlet pressure (15 psi) at 80 °C, 2.75 bar max. inlet pressure (40 psi) at 60 °C, 4.8 bar max. differential pressure (70 psid) at 20 °C, 5.5 bar max. inlet pressure (80 psi) at 23 °C, 80 psig max. inlet pressure
reg. compliance meets FDA 21 CFR 177-182 (all component materials)	reg. compliance meets FDA 21 CFR 177-182 (all component materials)	reg. compliance meets FDA 21 CFR 177-182 (all component materials)	reg. compliance meets FDA 21 CFR 177-182 (all component materials)
manufacturer/tradename Opticap^®	manufacturer/tradename Opticap^®	manufacturer/tradename Opticap^®	manufacturer/tradename Opticap^®

General description

Cartridge Type: Liquid

Device Configuration: Capsule

Packaging

Double Easy-Open bag

Preparation Note

Sterilization Method:
3 autoclave cycles of 30min at 126°C; not in-line steam sterilizable

This product was manufactured with a media combination which meets the criteria for a "non-fiber releasing" filter as defined in 21CFR210.3(b)(6).

Analysis Note

Gravimetric Extractables: ≤ 55mg per capsule after 24 hours in water at controlled room temperature.

Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥2L

Other Notes

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 installation section of OPTICAP^® XL Capsules and OPTICAP^® XLT Capsules user guide
Storage Statement: Store in dry location
Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations

Legal Information

CLARIGARD is a registered trademark of Merck KGaA, Darmstadt, Germany

OPTICAP is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class Code

10-13 - German Storage Class 10 to 13

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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Opticap® XL Capsule Filter