Identity
- Trade Name
- NAR FDA UDI
- Generic Name
- Cricothyrotomy kit, single-use FDA UDI
- Model / Reference
- 85-4267 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00842209127481 FDA UDI
- FDA Product Code
- OGP FDA UDI
- GMDN Term
- Cricothyrotomy kit, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5800 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
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: Cricothyrotomy kit, single-use
A comprehensive guide to the NAR cricothyrotomy kit, designed for emergency situations. Learn about its features, regulatory compliance, and how it's used in medical settings.
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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 II | Pending data |
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Manufacturer
- Manufacturer
- North American Rescue, Llc.
Sources (1)
- FDA UDI c9752e15-e590-4960-9850-fc14bb2aaba3 32 fields · synced Jun 20, 2026