KVGLS3TTT1 - Merck - Filters and Filtration - Chromatography - Lab supplies

: Catalog No. KVGLS3TTT1

Part No. KVGLS3TTT1
Supplier Merck KGaA

Opticap® Sterile XLT30 Durapore® 0.22 µm1-1/2 in. TC

Net Price

1409

Availability

4 weeks

PROPERTIES

Bacterial Endotoxins

Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
Bacterial Retention

Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology.
Cartridge Nominal Length

30 in. (75 cm)
Catalogue Number

KVGLS3TTT1
Chemistry

Polyvinylidene Fluoride (PVDF)
Device Configuration

Capsule
Device Material

Gamma-stable polypropylene
Device Size

30 in.
Diameter

10.7 cm (4.2 in.)
Filtration Area

2.17 m²
Good Manufacturing Practices

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

The extractables level was equal to or less than 75 mg per capsule after 24 hours in water at controlled room temperature.
Housing Material

Polypropylene (PP)
Indirect Food Additive

All component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182.
Inlet Connection

Sanitary Flange
Inlet Connection Diameter

1-1/2 in.
Inlet to Outlet Width

15.2 cm (6.0 in.)
Length

30 in. (75 cm)
Material Package

Double Easy-Open bag
Material Size

1
Maximum Differential Pressure, bar (psid)

Forward: 5.5 bar (80 psid) @ 25 °C; 1.7 bar (25 psid) @ 80 °C. Reverse: 3.5 bar (50 psid) @ 25 °C, intermittent
Maximum Inlet Pressure (psig)

80 psig
Maximum Inlet Pressure, bar (psi)

5.5 bar (80 psi) @ 23 °C; 2.8 bar (40 psi) @ 60 °C; 1.0 bar (15 psi) @ 80 °C
Maximum Inlet Temperature

25 °C
Media

Durapore®
Non-Fiber Releasing

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).
Outlet Connection

Sanitary Flange
Outlet Connection Diameter

1-1/2 in.
Oxidizable Substances

Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥3 L
Pore Size

0.22 µm
Seal Material

Lead O-ring: Silicone-coated EPDM, Outer O-ring: Silicone
Sterility

Sterile
Sterilization

3 autoclave cycles of 60 min @ 123 °C; not in-line steam sterilizable
Support Material

Polyester
Trade Name

Opticap®
USP Bacterial Endotoxins

A sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.
Vent Cap Material

Polypropylene (PP)
Wettability

Hydrophilic
Width

15.2 cm (6.0 in.)

DESCRIPTION

Genuine product