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Merck

KW19A04TT3

Milligard® 1.2 µm, Opticap® XL Capsule

inlet connection diam. 1.5 in., Opticap® XL 4, pore size 1.2 μm, cartridge nominal length 4 in. (10 cm)

동의어(들):

Opticap XL4 Milligard 1.2 μm 1-1/2 in. TC/TC

조직 및 계약 가격을 보려면 로그인를 클릭합니다.

크기 선택

제품정보 (DICE 배송 시 비용 별도)

eCl@ss:
32031610
UNSPSC Code:
23151806

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제품 이름

Milligard® 1.2 µm, Opticap® XL Capsule, inlet connection diam. 1.5 in., Opticap® XL 4, pore size 1.2 μm, cartridge nominal length 4 in. (10 cm)

material

mixed cellulose esters (MCE)
polyester support
polypropylene
polypropylene housing
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 4

feature

hydrophilic

manufacturer/tradename

Opticap®

parameter

1.0 bar max. inlet pressure (15 psi) at 80 °C
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
5.5 bar max. inlet pressure (80 psi) at 23 °C
80 psig max. inlet pressure

technique(s)

prefiltration: suitable

L

19.6 cm (7.7 in.)

W

3.3 in.

cartridge nominal length

4 in. (10 cm)

diam.

12.5 cm (4.9 in.)

filtration area

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

gravimetric extractables

≤25 mg/capsule

matrix

Milligard®

pore size

1.2 μm nominal pore size
1.2 μm pore size

input

sample type liquid

fitting

inlet sanitary flange
 outlet sanitary flange
 (38 mm (1 1/2 in.) Sanitary Flange Inlet and Outlet)

Quality Level

400

Analysis Note

Gravimetric Extractables: after 24 hours in water at controlled room temperature
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥1 L

Disclaimer

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.

Features and Benefits

Filter Grade: Standard Milligard® Media
Format: Single Layer

General description

Device Configuration: Capsule

Other Notes

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 installation section of OPTICAP® XL Capsules and OPTICAP® XLT Capsules user guide
  • Storage Statement: Store in dry location
  • Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations.

Replaces: KW1904TC1
These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.

Packaging

Double Easy-Open bag

Preparation Note

Sterilization Method
3 autoclave cycles of 30 min @ 121 °C; not in-line steam sterilizable
This product was manufactured with a media combination which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).

Legal Information

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

저장 등급

4.1B - Flammable solid hazardous materials

wgk

WGK 3

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국제 무역 품목 번호

SKUGTIN
KW19A04TT304053252721014

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