Merck, KVGLA04TT3, Durapore® 0.22 µm, Opticap® XL Capsule

Quality Level: 400

material: PVDF membrane, polypropylene housing, polypropylene support, polypropylene vent cap, silicone seal

reg. compliance: meets FDA Indirect Food Additive requirements cited in 21 CFR 177-182 (all component materials)

sterility: non-sterile

sterilization compatibility: autoclavable compatible

product line: Opticap^® XL

feature: hydrophilic

manufacturer/tradename: Durapore^®

parameter: 1.0 bar max. differential pressure (15 psid) at 80 °C (Forward), 1.0 bar max. inlet pressure (15 psi) at 80 °C, 3.4 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 25 °C

technique(s): sterile filtration: suitable

device L: 4 in. (10 cm)

filtration area: 0.19 m²

inlet connection diam. 1.5 in.

inlet to outlet W: 19.6 cm (7.7 in.)

outlet connection diam. 1.5 in.

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

gravimetric extractables: ≤10 mg/capsule

matrix: Durapore^®

pore size: 0.22 μm

input: sample type liquid

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

fitting: 38 mm (1 1/2 in.) inlet sanitary flange, 38 mm (1 1/2 in.) outlet sanitary flange