CTGB01TP3

Cartouche Aerex^® 0,2 µm

pore size 0.2 μm, cartridge nominal length 10 in. (25 cm), Code 0 (2-222; O-rings)

• Synonyme(s) : Aerex CTGB Cartridge Filter 10 in. 0.2 µm Code 0
• Code UNSPSC : 23151806
• eCl@ss : 32031690

Propriétés

• Matériaux: PTFE ; polypropylene ; polypropylene support; silicone seal
• Niveau de qualité: 400
• Stérilité: non-sterile
• Mode de stérilisation compatible: steam-in-place compatible
• Gamme de produits: Aerex^®
• Caractéristiques: hydrophobic
• Fabricant/nom de marque: Aerex^®
• Paramètres: ≤15 mL/min nitrogen diffusion at 690 mbar (10 psig) and 23 °C (in 60/40% IPA/water); 0.35 bar max. differential pressure (5 psid) at 145 °C (Forward); 0.35 bar max. inlet pressure (5 psi) at 145 °C (Forward); 1.7 bar max. differential pressure (25 psid) at 80 °C (Forward); 1.7 bar max. inlet pressure (25 psi) at 80 °C (Forward); 5.2 bar max. differential pressure (75 psid) at 25 °C (Reverse; intermittent); 5.2 bar max. inlet pressure (75 psi) at 25 °C (Reverse); 6.9 bar max. differential pressure (100 psid) at 25 °C (Forward); 7 bar max. inlet pressure (100 psi) at 25 °C (Forward)
• Technique(s): gas filtration: suitable
• Longueur: 10 in.
• Largeur: 2.7 in.
• Longueur nominale des cartouches: 10 in. (25 cm)
• Diamètre: 6.9 cm (2.7 in.)
• Surface de filtration: 0.65 m²
• Impuretés: ≤0.5 EU/mL bacterial endotoxins (LAL test, Aqueous extraction); <0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• Extractibles par gravimétrie: ≤35 mg/cartridge
• Matrice: Aerex^®
• Dimension de pores: 0.2 μm pore size
• Entrée: sample type gas
• Point de bulle: ≥900 mbar (13 psig), nitrogen with 60/40% IPA/water at 23 °C
• Code de la cartouche: Code 0 (2-222; O-rings)

Description

Description générale

Device Configuration: Cartridge

Caractéristiques et avantages

This product has been qualified to retain a ΦX174 virus aerosol challenge of 10⁸ to 10¹⁰ PFU at an air flow rate of 50 SCFM per 10-inch cartridge after 50 steam-in-place cycles at 145 °C.

Conditionnement

Easy-Open bag

Autres remarques

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 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.

Qualité

The membrane has been qualified to retain bacteria when challenged for 21 days with a minimum Brevundimonas diminuta aerosol concentration of 1 x 10⁷ CFU/cm².

Notes préparatoires

Sterilization Method
200 (150 forward/50 reverse) SIP cycles of 30 min @ 145 °C; SIP up to 165 hours in forward direction @ 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).

Remarque sur l'analyse

Gravimetric Extractables: after 24 hours in a 70/30% IPA/water mixture at controlled room temperature

HydroCorr: ≤0.40 mL/min per 10-inch cartridge with water @ 1380 mbar (20 psig)

Informations légales

AEREX is a registered trademark of Merck KGaA, Darmstadt, Germany