Resp-O2 Disposable Guedel Airway, 80 mm, Adult Small, Green

GUDID 00840117340381

Dynarex Corporation

Oropharyngeal airway, single-use

• Primary Device ID: 00840117340381
• NIH Device Record Key: 8b67c9ca-cfa1-469f-9e2f-93a82e3e0900
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Resp-O2 Disposable Guedel Airway, 80 mm, Adult Small, Green
• Version Model Number: 36319
• Company DUNS: 008124539
• Company Name: Dynarex Corporation
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840117340381 [Primary]
GS1	00840117340541 [Package]; Package: Box [10 Units]; In Commercial Distribution
GS1	00840117340633 [Package]; Contains: 00840117340541; Package: Shipper [50 Units]; In Commercial Distribution

FDA Product Code

• CAE: Airway, Oropharyngeal, Anesthesiology

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: 2024-12-09
• Device Publish Date: 2024-11-29

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