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KTGRA04TH3

Aervent^® 0.2 µm, Opticap^® XL Capsule

Name: Aervent<SUP>&#174;</SUP> 0.2 µm, Opticap<SUP>&#174;</SUP> XL Capsule
Brand: MM

inlet connection diam. 1.5 in., Opticap^® XL 4, pore size 0.2 μm, cartridge nominal length 4 in. (10 cm)

동의어(들):

Aervent^® 0.2 µm, Opticap^® XL Capsule, Opticap XL 4 with Aervent - 4" 0.2um TC/HB 3pk

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제품정보 (DICE 배송 시 비용 별도)

eCl@ss:

32031690

UNSPSC Code:

23151806

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속성

제품 이름

Opticap^® XL 4 CapsuleMedia: Aervent^® 0.2 µm, Chemistry: Hydrophobic Polytetrafluoroethylene (PTFE)Inlet: 1-1/2 in. Sanitary FlangeOutlet: 9/16 in. Hose BarbMax Operating Pressure: 80 psi @ 25 °C

Quality Level

400

material

PTFE , polypropylene , polypropylene housing, polypropylene vent cap, silicone seal

sterility

non-sterile

sterilization compatibility

autoclavable compatible

product line

Opticap^® XL 4

feature

hydrophobic

manufacturer/tradename

Opticap^®

parameter

1.0 bar max. differential pressure (15 psid) at 80 °C (Forward), 1.0 bar max. inlet pressure (15 psi) at 80 °C, 2.75 bar max. inlet pressure (40 psi) at 60 °C, 25 °C max. inlet temp., 4.1 bar max. differential pressure (60 psid) at 25 °C (Reverse; intermittent), 5.5 bar max. differential pressure (80 psid) at 25 °C (Forward), 5.5 bar max. inlet pressure (80 psi) at 25 °C, 80 psig max. inlet pressure

technique(s)

gas filtration: suitable

L

7.7 in.

W

3.3 in.

cartridge nominal length

4 in. (10 cm)

diam.

8.4 cm (3.3 in.)

filtration area

0.21 m²

inlet connection diam.

1.5 in.

outlet connection diam.

9/16 in.

impurities

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

gravimetric extractables

≤15 mg

matrix

Aervent^®

pore size

0.2 μm pore size

fitting

1/4 in. drain/vent hose barb (with double O-ring Seal), inlet sanitary flange, outlet hose barb, (38 mm (1 1/2 in.) Sanitary Flange Inlet and 14 mm (9/16 in.) Hose Barb Outlet)

설명

General description

Device Configuration: Capsule

Packaging

Double Easy-Open bag

Preparation Note

Sterilization Method
3 autoclave cycles of 60 min @ 123 °C; not in-line steam sterilizable

This product was manufactured with a PTFE 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 a 70/30% IPA/water mixture at controlled room temperature

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 Steam Sterilization & Integrity Testing Procedures guide and first page of Visual Inspection Guide
Storage Statement: Store in dry location
Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations.

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

Legal Information

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

ASTM is a registered trademark of American Society for Testing and Materials

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

Disclaimer

EMD Millipore Corporation certifies that this product complies with the European Pressure Equipment Directive, 97/23/EC of 29 May 1997. This product has been classified under Article 3 § 3 of the Pressure Vessel Directive. It has been designed and manufactured in accordance with sound engineering practice to ensure safe use. In compliance with Article 3 § 3 of this Pressure Vessel Directive, this product does not bear the CE mark.

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SKU	GTIN
KTGRA04TH3	04053252652172