AMBU Co2 Detector

GUDID 05707480133758

Carbon Dioxide Detector

WESTMED, INC.

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• Primary Device ID: 05707480133758
• NIH Device Record Key: 40ec88d2-683d-4ec0-ae66-33e26c34fb42
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AMBU Co2 Detector
• Version Model Number: 000-172-712
• 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: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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	05707480101054 [Primary]
GS1	05707480133758 [Package]; Contains: 05707480101054; Package: [12 Units]; In Commercial Distribution

FDA Product Code

• CCK: Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase

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: 2022-08-23
• Device Publish Date: 2022-08-15

On-Brand Devices [AMBU Co2 Detector]

• 05707480133772: Carbon Dioxide Detector w/ Adapter
• 05707480133758: Carbon Dioxide Detector