Composite Respiratory Kit

GUDID 10709078005708

O2 Composite Kit

WESTMED, INC.

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• Primary Device ID: 10709078005708
• NIH Device Record Key: bba6cdda-d4c3-4521-8084-9447e6a9a089
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Composite Respiratory Kit
• Version Model Number: 0797
• Company DUNS: 092673953
• Company Name: WESTMED, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00709078005701 [Primary]
GS1	10709078005708 [Package]; Contains: 00709078005701; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• CAT: Cannula, Nasal, Oxygen

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: 2018-06-18
• Device Publish Date: 2018-05-16

On-Brand Devices [Composite Respiratory Kit]

• 10709078005708: O2 Composite Kit
• 10709078003612: 1 - Packaged 50' O2 Tubing (0052), 6 - Packaged Soft Cannula with 7' Tubing (0556), 1 - Barbed C
• 10709078005968: 0798
• 10709078007788: Composite Respiratory Kit