KVVLA3STT1

Durapore^® 0.1 µm, Opticap^® XLT Capsule

cartridge nominal length 30 in. (15 cm), Opticap^® XLT 30, filter diam. 5.7 in. (14.5 cm), pore size 0.1 μm

• UNSPSC Code: 23151806

Properties

• material: polypropylene device; polypropylene housing; polypropylene support; polypropylene vent cap
• Quality Level: 400
• reg. compliance: meets FDA 21 CFR 177-182 (all component materials)
• sterility: non-sterile
• Sterilization Compatibility: autoclavable compatible
• product line: Opticap^® XLT 30
• feature: hydrophilic
• manufacturer/tradename: Opticap^®
• parameter: max. inlet temp. at 25 °C; ≤60 mL/min air diffusion at 3.9 bar (56 psig) (in water); 1.7 bar max. differential pressure (25 psid) at 80 °C (Forward); 2.8 bar max. inlet pressure (40 psi) at 60 °C; 3.5 bar max. differential pressure (50 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 23 °C; 80 psig max. inlet pressure
• technique(s): sterile filtration: suitable
• L: 34.3 in.
• W: 6.0 in.
• cartridge nominal length: 30 in. (15 cm)
• device size: 30 in.
• filter diam.: 5.7 in. (14.5 cm)
• filter filtration area: 2.1 m²
• inlet to outlet width: 34.3 in. (87.1 cm)
• impurities: ≤0.5 EU/mL bacterial endotoxins (LAL test, aqueous extraction); <0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• matrix: Durapore^®
• pore size: 0.1 μm pore size
• bubble point: ≥4830 mbar (70 psig), air with water at 23 °C
• fitting: 1/4 in. drain/vent connection (with double O-ring Seal); (38 mm (1 1/2 in.) Sanitary Flange Inlet and Outlet)

Description

General description

Device Configuration: Cartridge
Cartridge Type: Liquid

Features and Benefits

T-line/Gauge Port: T-line

Preparation Note

Sterilization Method: Capsule integrity was maintained after 3 autoclave cyclces of 60 minutes at 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: ≤ 75 mg per capsule after 24 hours in water 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 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

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

Legal Information

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

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

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