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Nar

FDA UDI

Class II (US FDA UDI)

by North American Rescue, Llc.

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.

Similar devices

Also classified as Cricothyrotomy kit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c9752e15-e590-4960-9850-fc14bb2aaba3 32 fields · synced Jun 20, 2026