Identity
- Trade Name
- Airmax FDA UDI
- Generic Name
- Nasal breathing aid, internal, reusable FDA UDI
- Model / Reference
- Nasal Dilator - Medium - Clear FDA UDI
Identifiers
- Catalog Number
- 2350 FDA UDI
- Primary DI / UDI-DI
- 00033732023504 FDA UDI
- FDA Product Code
- LWF FDA UDI
- GMDN Term
- Nasal breathing aid, internal, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.3900 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Nasal breathing aid, internal, reusable
Airmax by Mckeon Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Nasal breathing aid, internal, reusable.
- Somnics — SOMNICS, INC. · Class I
- Somnics — SOMNICS, INC. · Class I
- iNAP — SOMNICS, INC. · Class II
- iNAP — SOMNICS, INC. · Class II
- Somnics — SOMNICS, INC. · Class I
- Somnics — SOMNICS, INC. · Class I
- Airmax — Mckeon Products · Class I
- Airmax — Mckeon Products · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Mckeon Products
Sources (1)
- FDA UDI 06a23248-bd4b-4d33-bee9-0f6efac2298c 33 fields · synced Jun 1, 2026