KHGLG3TTT1

Multilayer Durapore^® 0.45/0.22 µm, Opticap^® XLT Capsule

Opticap^® XLT 30, inlet connection diam. 1.5 in., pore size 0.45/0.22 μm, cartridge nominal length 30 in. (75 cm)

• Synonym(s): Opticap Gamma Compatible Multilayer XLT30 Durapore0.45/0.22 μm 1-1/2 in. TC
• UNSPSC Code: 23151806

Properties

• material: PVDF ; polyester support; polyethylene support; polypropylene ; polypropylene housing; polypropylene vent cap; silicone seal
• Quality Level: 400
• reg. compliance: meets FDA Indirect Food Additive requirements cited in 21 CFR 177-182 (all component materials)
• sterility: non-sterile
• sterilization compatibility: gamma compatible
• product line: Opticap^® XLT 30
• feature: gamma compatible; hydrophilic
• manufacturer/tradename: Opticap^®
• parameter: ≤45.0 mL/min air diffusion at 2.75 bar (40 psig) and 23 °C (in water); 1.0 bar max. inlet pressure (15 psi) at 80 °C; 1.05 bar max. differential pressure (15 psid) at 80 °C (Forward); 2.75 bar max. inlet pressure (40 psi) at 60 °C; 25 °C max. inlet temp.; 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: 87.1 cm (34.3 in.)
• W: 7.8 in.
• cartridge nominal length: 30 in. (75 cm)
• diam.: 10.7 cm (4.2 in.)
• filtration area: 1.81 m²
• inlet connection diam.: 1.5 in.
• inlet to outlet W: 15.2 cm (6.0 in.)
• outlet connection diam.: 1.5 in.
• impurities: ≤0.25 EU/mL bacterial endotoxins (LAL test, Aqueous extraction); <0.25 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• matrix: Multilayer Durapore^®
• pore size: 0.45/0.22 μm pore size
• input: sample type liquid
• bubble point: ≥3450 mbar (50 psig), air with water at 23 °C
• fitting: 1/4 in. drain/vent hose barb (with double O-ring Seal); inlet sanitary flange; outlet sanitary flange; (38 mm (1 1/2 in.) Sanitary Flange Inlet and Outlet)

Description

General description

Device Configuration: Capsule

T-line/Gauge Port: T-line

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
Gamma compatible to 45 kGy; 3 autoclave cycles of 60 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.

TOC/Conductivity
After sterilization and a controlled water flush, samples exhibited less than 500 ppb TOC per USP <64> and less than 1.3 µS/cm per USP <64> at 25 ºC.

Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥4.5 L

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