Identity
- Trade Name
- NAR FDA UDI
- Generic Name
- First aid kit, non-medicated, single-use FDA UDI
- Model / Reference
- 85-4089 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00842209125753 FDA UDI
- GMDN Term
- First aid kit, non-medicated, single-use FDA UDI
Classification
- 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
No
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 device is a convenient and non-medicated first aid kit suitable for emergency situations, used by various public settings. It's designed to provide immediate treatment in the event of an injury or accident.
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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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- North American Rescue, Llc.
Sources (1)
- FDA UDI 715171d6-cd59-4430-b322-ce41b4f49faa 32 fields · synced Jul 14, 2026