Airmax 2350

GUDID 00033732023504

McKeon Products, Inc.

Nasal breathing aid, internal, reusable

• Primary Device ID: 00033732023504
• NIH Device Record Key: 06a23248-bd4b-4d33-bee9-0f6efac2298c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Airmax
• Version Model Number: Nasal Dilator - Medium - Clear
• Catalog Number: 2350
• Company DUNS: 006522122
• Company Name: McKeon Products, 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: false
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00033732023504 [Primary]

FDA Product Code

• LWF: Dilator, Nasal

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: 2022-10-17
• Device Publish Date: 2022-10-07

On-Brand Devices [Airmax]

• 00033732023504: Nasal Dilator - Medium - Clear
• 00033732023498: Nasal Dilator - Medium - Orange
• 00033732023252: Nasal Dilator Trial Pack (1 small + 1 medium)
• 00033732023023: Nasal Dilator - Small - Clear
• 00033732023016: Nasal Dilator - Small - Blue