Identity
- Trade Name
- NAR Kit FDA UDI
- Generic Name
- First aid kit, non-medicated, single-use FDA UDI
- Device Name
- KIT, CCR-MEDIC TRAUMA PACK - DUC FDA UDI
- Model / Reference
- 80-0096 FDA UDI
- Description
- KIT, CCR-MEDIC TRAUMA PACK - DUC FDA UDI
Identifiers
- Catalog Number
- 80-0096 FDA UDI
- Primary DI / UDI-DI
- 00842209100446 FDA UDI
- GMDN Term
- First aid kit, non-medicated, single-use FDA UDI
Classification
- Commercial Distribution
- Not 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
MR Unsafe FDA UDI
NAR Kit by North American Rescue, Llc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 5d844b6d-ba58-49ba-a4ed-69ee4d05e5cf 35 fields · synced Jun 8, 2026