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Merck
CN

KZRVA1TTT1

Millipore

Opticap XLT10 Viresolve NFR 1-1/2 in. TC/TC

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About This Item

UNSPSC Code:
23151806
eCl@ss:
32031690

Key Documents

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material

polyethersulfone
polypropylene
polypropylene support
polypropylene vent cap
silicone seal

Quality Level

400

description

T-line

product category

capsule filters

parameter

≤16 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

38 cm (15 in.)

device size

10 in.

filtration area

0.43 m2

hold-up volume

175 mL

inlet connection diam.

1 1/2 in.

outlet W

15.2 cm (6.0 in.)

outlet connection diam.

1-1/2 in.

size

600-1200 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

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

The extractables level was equal to or less than 35 mg after a 10 minute 1.5 LPM/ft² flush and 24 hours in water at controlled room temperature.
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥4 L

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

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.

Regulatory Information

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