Nar

FDA UDI

Class I (US FDA UDI)

by North American Rescue, Llc.

Identity

Trade Name: NAR FDA UDI
Generic Name: First aid kit, non-medicated, single-use FDA UDI
Model / Reference: 35-0025 FDA UDI

Identifiers

Catalog Number: 35-0025 FDA UDI
Primary DI / UDI-DI: 00842209125784 FDA UDI
FDA Product Code: OHO FDA UDI
LGZ FDA UDI
BSB 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
880.5725 FDA UDI
864.9205 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: First aid kit, non-medicated, single-use Conduction blood/fluid warmer

Nar by North American Rescue, Llc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 041ed251-f956-408b-96d3-dbc13a49eaa8 33 fields · synced May 31, 2026