Hepa Filter

GUDID 10709078014007

Hepa Filter W/CO2 port (TwinMed)

WESTMED, INC.

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• Primary Device ID: 10709078014007
• NIH Device Record Key: efb8d760-97ff-4cb9-840c-ca2392ed934d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hepa Filter
• Version Model Number: 1002217
• Company DUNS: 092673953
• Company Name: WESTMED, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00709078014000 [Primary]
GS1	10709078014007 [Package]; Contains: 00709078014000; Package: [50 Units]; In Commercial Distribution

FDA Product Code

• CAH: Filter, Bacterial, Breathing-Circuit

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-04-08
• Device Publish Date: 2022-03-31

On-Brand Devices [Hepa Filter]

• 10709078002240: *HEPA Filter with Port and Elbow (6224)
• 00709078001567: w/o CO2 Port
• 10709078014007: Hepa Filter W/CO2 port (TwinMed)