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Merck
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CTGR73TP1

Millipore

Aervent® 0.2 µm, Cartridge

pore size 0.2 μm, cartridge nominal length 30 in. (76 cm), Code 7

Synonym(s):

Aervent CTGR Cartridge Filter 30 in. 0.2 µm Code 7

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1 EACH
CN¥648.15
1 KG
CN¥2,277.35

About This Item

UNSPSC Code:
23151806
eCl@ss:
32031690

CN¥648.15


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material

PTFE
polypropylene
polypropylene support
silicone seal

Quality Level

sterility

non-sterile

Sterilization Compatibility

steam-in-place compatible

product line

Aervent®

feature

hydrophobic

manufacturer/tradename

Aervent®

parameter

≤72 mL/min nitrogen diffusion at 970 mbar (14 psig) and 23 °C (in 70/30% IPA/water)
1.7 bar max. inlet pressure (25 psi) at 80 °C
1.8 bar max. differential pressure (25 psid) at 80 °C (Forward)
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)

technique(s)

gas filtration: suitable

L

30 in.

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This Item
W2186181084215W269301
grade

FG, Kosher, Halal

grade

FG, Halal, Kosher

grade

pharmaceutical primary standard

grade

FG, Fragrance grade, Halal, Kosher

organoleptic

green; waxy; fruity; sweet

organoleptic

green; fruity; sweet

organoleptic

-

organoleptic

apple; ethereal

biological source

synthetic

biological source

synthetic

biological source

-

biological source

synthetic

food allergen

no known allergens

food allergen

no known allergens

food allergen

-

food allergen

no known allergens

agency

meets purity specifications of JECFA

agency

meets purity specifications of JECFA

agency

-

agency

(EU Regulation 1223/2009), (follows IFRA guidelines), meets purity specifications of JECFA

documentation

see Safety & Documentation for available documents

documentation

see Safety & Documentation for available documents

documentation

-

documentation

see Safety & Documentation for available documents

General description

Device Configuration: Cartridge

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
150 (100 forward/50 reverse) SIP cycles of 30 min @ 145 °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: ≤2.3 mL/min @ 2.6 bar (38 psig) per 30 in cartridge
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.

Legal Information

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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