← Back to catalogue

Nar

FDA UDI

Class N (US FDA UDI)

by North American Rescue, Llc.

Identity

Trade Name
NAR FDA UDI
Generic Name
First aid kit, medicated FDA UDI
Model / Reference
80-1824 FDA UDI

Identifiers

Catalog Number
80-1824 FDA UDI
Primary DI / UDI-DI
00842209135554 FDA UDI
FDA Product Code
LRR FDA UDI
GMDN Term
First aid kit, medicated FDA UDI

Classification

Device Class
N 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

Yes

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, medicated

Explore the NAR medical device, a convenient collection of equipment and pharmaceuticals for emergency treatment. This reusable kit is designed for public use in various settings, providing a rapid initial response to injuries.

Similar devices

Also classified as First aid kit, medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 790b13b7-1fc5-4a7b-bf16-bc9d94e27448 33 fields · synced Jul 14, 2026