Portex

Portex - 225-2531-805

A screening device intended to be installed within a suction system and which has a membrane pore size small enough to retain bacterial pathogens, thus preventing the environment from becoming infected and decreasing the risk of cross-infection to subsequent patients. It is typically directly connected to the suction system collection bottle/canister, or as a common filter serving more than one bottle/canister through a switching mechanism, or in a tubing line between the suction bottle/canister and the suction pump, or at the suction pump exhaust where driving gases are discarded. This is a single-use device.

No Data Available

No Data Available

Device Sterile: False

Sterilization Prior To Use: False

Sterilization Methods: No Data Available

Code: KDQ

Device Name: Bottle, Collection, Vacuum

Device Class: 2

Physical State: N/A

Definition: N/A

Submission Type ID: 4

Review Panel: HO

Review Code: N/A

Technical Method: N

Gmp Exempt Flag: N/A

Life Sustain Support Flag: N

Unclassified Reason: N/A

Implant Flag: N

Target Area: N/A

Regulation Number: 880.6740

Third Party Flag: N

Medical Specialty: HO

Device Id: 50351688429733

Device Type: Package

DeviceId Issuing Agency: GS1

Contains DI Number: 10351688429735

Package Quantity: 20

Package Discontinue Date: N/A

Package Status: In Commercial Distribution

Package Type: BAG

Device Id: 10351688429735

Device Type: Primary

DeviceId Issuing Agency: GS1

Contains DI Number: N/A

Package Quantity: N/A

Package Discontinue Date: N/A

Package Status: N/A

Package Type: N/A

Device Id: 30351688429739

Device Type: Package

DeviceId Issuing Agency: GS1

Contains DI Number: 50351688429733

Package Quantity: 200

Package Discontinue Date: N/A

Package Status: In Commercial Distribution

Package Type: BOX