콘텐츠로 건너뛰기
Merck

주요 문서

모든 문서 보기

KTGRA10TT1

Aervent® 0.2 µm, Opticap® XL Capsule

inlet connection diam. 1.5 in., Opticap® XL 10, pore size 0.2 μm, cartridge nominal length 10 in. (25 cm)

동의어(들):

Aervent® 0.2 µm, Opticap® XL Capsule, Aervent KTGR Opticap XL10 Capsule

조직 및 계약 가격을 보려면 로그인를 클릭합니다.

크기 선택

보기 변경

제품정보 (DICE 배송 시 비용 별도)

eCl@ss:
32031690
UNSPSC Code:
23151806
기술 서비스
도움이 필요하신가요? 저희 숙련된 과학자 팀이 도와드리겠습니다.
도움 문의

제품 이름

Opticap® XL 10 CapsuleMedia: Aervent® 0.2 µm, Chemistry: Hydrophobic Polytetrafluoroethylene (PTFE)Inlet: 1-1/2 in. Sanitary FlangeOutlet: 1-1/2 in. Sanitary FlangeMax. Operating Pressure: 80 psi @ 25 °C

Quality Level

400

material

PTFE , polypropylene , polypropylene housing, polypropylene support, polypropylene vent cap, silicone seal

sterility

non-sterile

sterilization compatibility

autoclavable compatible

product line

Opticap® XL 10

feature

hydrophobic

manufacturer/tradename

Aervent®

parameter

≤24 mL/min nitrogen diffusion at 970 mbar (14 psig) and 23 °C (in 70/30% IPA/water), 1.0 bar max. differential pressure (15 psid) at 80 °C (Forward), 1.0 bar max. inlet pressure (15 psi) at 80 °C (Forward), 2.8 bar max. inlet pressure (40 psi) at 60 °C (Forward), 25 °C max. inlet temp., 4.1 bar max. differential pressure (60 psid) (Reverse; intermittent), 4.1 bar max. inlet pressure (60 psi) (Reverse; Intermittent), 5.5 bar max. differential pressure (80 psid) at 25 °C (Forward), 5.5 bar max. inlet pressure (80 psi) at 25 °C (Forward), 80 psig max. inlet pressure

technique(s)

gas filtration: suitable

L

33.5 cm (13.2 in.)

W

4.2 in.

cartridge nominal length

10 in. (25 cm)

diam.

10.7 cm (4.2 in.)

filtration area

0.65 m2

inlet connection diam.

1.5 in.

inlet to outlet W

33.5 cm (13.2 in.)

outlet connection diam.

1.5 in.

impurities

<0.25 EU/mL USP bacterial endotoxins (LAL test, aqueous extraction)

gravimetric extractables

≤45 mg/cartridge

matrix

Aervent®

pore size

0.2 μm pore size

input

sample type gas

bubble point

≥1100 mbar (16 psig), nitrogen with 70/30% IPA/water at 23 °C

fitting

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

General description

Device Configuration: Capsule

Features and Benefits

Rated for aerosol retention of a total challenge of 108–1010 plaque forming units of ΦX-174 virus particles at 85 Nm3/h (50 SCFM) per cartridge.

Packaging

Double Easy-Open bag

Preparation Note

Sterilization Method
30 autoclave cycles of 30 min @ 135 °C
This product was manufactured with a PTFE membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).

Analysis Note

Bacterial Retention
Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology.
Gravimetric Extractables: after 24 hours in a 70/30% IPA/water mixture at controlled room temperature
HydroCorr: ≤0.75 mL/min @ 2.6 bar (38 psig) per sample
Retains Brevundimonas diminuta liquid aerosol for 21 days at a minimum challenge of 10⁷ CFU/cm²

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 Steam Sterilization & Integrity Testing Procedures guide and first page of Visual Inspection Guide
  • Storage Statement: Store in dry location
  • Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations.

Replaces: SN2M027A6

Legal Information

AERVENT is a registered trademark of Merck KGaA, Darmstadt, Germany
ASTM is a registered trademark of American Society for Testing and Materials
OPTICAP is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

EMD Millipore Corporation certifies that this product complies with the European Pressure Equipment Directive, 2014/68/EU of 15 May 2014. This product has been classified under Article 4 § 3 of the Directive 2014/68/EU. It has been designed and manufactured in accordance with sound engineering practice to ensure safe use. In compliance with Article 4 § 3 of the Directive 2014/68/EU, this product does not bear the CE mark.

Still not finding the right product?

Explore all of our products under

시험 성적서(COA)

제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.

이 제품을 이미 가지고 계십니까?

문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

국제 무역 품목 번호

SKUGTIN
KTGRA10TT104053252392689