Identity
- Trade Name
- NAR FDA UDI
- Generic Name
- First aid kit, non-medicated, single-use FDA UDI
- Model / Reference
- 85-4847 FDA UDI
Identifiers
- Catalog Number
- 85-4847 FDA UDI
- Primary DI / UDI-DI
- 00842209134793 FDA UDI
- FDA Product Code
- OHO FDA UDI
- GMDN Term
- First aid kit, non-medicated, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4014 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: First aid kit, non-medicated, single-use
The NAR medical device is a convenient, single-use first aid kit without medicated substances, designed for emergency treatment in public settings. Developed by NORTH AMERICAN RESCUE, LLC, it's marketed as an essential tool for institutions and individuals alike.
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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 |
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Manufacturer
- Manufacturer
- North American Rescue, Llc.
Sources (1)
- FDA UDI 756abde9-196e-4d1d-b2bd-798309d75d70 33 fields · synced Jun 20, 2026