FORWARD Oral Airway Kit

GUDID 00850056748179

Oral Airway Kit that contains airway sizes 5, 6.5, 7, 8, 9, 10, and 12

INTEGRATED MEDCRAFT LLC

Intrauterine cannula, single-use

• Primary Device ID: 00850056748179
• NIH Device Record Key: e99305ee-11d0-4627-82c5-5293a02181a7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FORWARD Oral Airway Kit
• Version Model Number: 1011-40002
• Company DUNS: 107523667
• Company Name: INTEGRATED MEDCRAFT 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: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850056748179 [Primary]

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: 2025-01-07
• Device Publish Date: 2024-12-30

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