Intubation Guide Kit

GUDID 00860009615540

AIR Q KIT - SZ 5

Nar Medical Depot, LLC

General surgical procedure kit, non-medicated, single-use

• Primary Device ID: 00860009615540
• NIH Device Record Key: 1ceeb835-22fb-4ee7-bd04-d1fa62b79d8d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Intubation Guide Kit
• Version Model Number: 800-00047
• Company DUNS: 117667182
• Company Name: Nar Medical Depot, LLC
• 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: true
• 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: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860009615540 [Primary]

FDA Product Code

• OGK: Orotracheal Intubation Guide Kit

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: 2025-07-23
• Device Publish Date: 2025-07-15

On-Brand Devices [Intubation Guide Kit]

• 00860009615557: AIR Q KIT - SZ 4
• 00860009615540: AIR Q KIT - SZ 5
• 00860009615533: AIR Q KIT - SZ 3