Cannula

GUDID 10709078012751

Cannula, Adult, Divided, CO2/O2

WESTMED, INC.

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• Primary Device ID: 10709078012751
• NIH Device Record Key: cf101715-773f-4983-8751-c2700c1f0f25
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cannula
• Version Model Number: P185361
• 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: 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	00709078012754 [Primary]
GS1	10709078012751 [Package]; Contains: 00709078012754; Package: Case [100 Units]; In Commercial Distribution

FDA Product Code

• CAT: Cannula, Nasal, Oxygen
• 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: 2021-07-08
• Device Publish Date: 2021-06-30

On-Brand Devices [Cannula]

• 10709078011457: Adult Nasal Cannula W/ 7' KROT
• 10709078010870: CO2 Sampling Nasal Cannula, 15"
• 10709078012775: Cannula, Pediatric, Divided, CO2/O2
• 10709078012768: Cannula, Pediatric, Divided, CO2/O2
• 10709078012751: Cannula, Adult, Divided, CO2/O2
• 10709078012744: Cannula, Adult, Divided, CO2/O2
• 10709078012706: LoFlo Sample Line, Neo. Cannula
• 10709078012683: LoFlo Sample Line, Ped. Cannula
• 10709078012669: LoFlo Sample Line, Adult, Cannula