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Merck
CN

KZRVA2TTT1

Opticap® XLT 20 Capsule Media: Viresolve® NFR

Chemistry: Polyethersulfone (PES) Inlet: 1-1/2 in. Sanitary Flange Outlet: 1-1/2 in. Sanitary Flange T-line Max Operating Pressure: 80 psi @ 25 °C

别名:

Opticap XLT20 Viresolve NFR 1-1/2 in. TC/TC

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eCl@ss:
32031690
UNSPSC Code:
23151806

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产品名称

Opticap® XLT 20 Capsule Media: Viresolve® NFR, Chemistry: Polyethersulfone (PES) Inlet: 1-1/2 in. Sanitary Flange Outlet: 1-1/2 in. Sanitary Flange T-line Max Operating Pressure: 80 psi @ 25 °C

description

T-line with 1-1/2 in. Gauge Port

product category

capsule filters

parameter

≤32 mL/min air diffusion at 3.45 bar (50 psig) (in water), 25 °C max. inlet temp., 3.4 bar max. differential pressure (50 psid) (Reverse), 5.5 bar max. differential pressure (80 psid) (Forward), 5.5 bar max. inlet pressure (80 psi) at 23 °C, 80 psig max. inlet pressure

technique(s)

protein purification: suitable

L

63.5 cm (25 in.)

device size

20 in.

filtration area

0.854 m2

hold-up volume

325 mL

inlet connection diam.

1 1/2 in.

outlet W

15.2 cm (6.0 in.)

outlet connection diam.

1-1/2 in.

size

1200-2400 L

impurities

≤0.5 EU/mL Aqueous extraction (LAL test)

matrix

Viresolve® NFR

fitting

1/4 in. hose barb (double O-ring Seal), hose barb 1/4 in. (double O-ring Seal), inlet sanitary flange, inlet sanitary flange, outlet sanitary flange, outlet sanitary flange, 38 mm (1 1/2 in.) sanitary flange drain/vent, sanitary flange drain/vent 38 mm (1 1/2 in.)

suitability

suitable for endotoxin

material

polyethersulfone , polypropylene , polypropylene support, polypropylene vent cap, silicone seal

Quality Level

400

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General description

A sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.
After wetting, may be autoclaved for 3 cycles of up to 60 min at 125 °C, using liquid cycle, slow exhaust.

Packaging

Double Easy-Open bag

Analysis Note

Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥8 L
The extractables level was equal to or less than 70 mg after a 10 minute 1.5 LPM/ft² flush and 24 hours in water at controlled room temperature.

Other Notes

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.

Legal Information

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

Disclaimer

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

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