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Merck
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KWSCA2TTT1

Millipore

Milligard® 1.2/0.5 µm nominal, Opticap® XLT Capsule

inlet connection diam. 1.5 in., Opticap® XLT 20, pore size 1.2/0.5 μm, cartridge nominal length 20 in. (50 cm)

别名:

Opticap XLT20 Milligard 1.2/0.5 μm 1-1/2 in. TC/TC

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About This Item

分類程式碼代碼:
23151806
eCl@ss:
32031610

材料

mixed cellulose esters (MCE)
polyester support
polypropylene
polypropylene housing
polypropylene vent cap
silicone seal

品質等級

法律遵循

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

無菌

non-sterile

滅菌相容性

autoclavable compatible

產品線

Opticap® XLT 20

特點

hydrophilic

製造商/商標名

Opticap®

參數

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

技術

prefiltration: suitable

長度

62.5 cm (24.6 in.)

柱標稱長度

20 in. (50 cm)

過濾面積

1.38 m2

入口接頭直徑

1.5 in.

入口到出口寬度

15.2 cm (6.0 in.)

出口接頭直徑

1.5 in.

雜質

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

重量法萃取物

≤110 mg/capsule

基質

Milligard®

pore size

1.2/0.5 μm nominal pore size
1.2/0.5 μm pore size

輸入

sample type liquid

接頭

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

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一般說明

Device Configuration: 取样皿滤膜
T-line/Gauge Port: T-line

特點和優勢

Format: Double Layer

包裝

Double Easy-Open bag

其他說明

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

規格

Filter Grade: Standard Milligard® Media

準備報告

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).

分析報告

Gravimetric Extractables: after 24 hours in water at controlled room temperature
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥10 L

法律資訊

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

免責聲明

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.

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儲存類別代碼

4.1B - Flammable solid hazardous materials

水污染物質分類(WGK)

WGK 3


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