← Back to catalogue

Nar

FDA UDI

Class I (US FDA UDI)

by North American Rescue, Llc.

Identity

Trade Name
NAR FDA UDI
Generic Name
First aid absorbent pad/bandage FDA UDI
Device Name
DRESSING, EMERGENCY TRAUMA - 6" ABDOMINAL (12"x12") FDA UDI
Model / Reference
30-0012 FDA UDI
Description
DRESSING, EMERGENCY TRAUMA - 6" ABDOMINAL (12"x12") FDA UDI

Identifiers

Catalog Number
30-0012B FDA UDI
Primary DI / UDI-DI
00842209108923 FDA UDI
FDA Product Code
FQM FDA UDI
GMDN Term
First aid absorbent pad/bandage FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5075 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

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 absorbent pad/bandage

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

Similar devices

Also classified as First aid absorbent pad/bandage.

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 c841c4c4-ef9f-4957-812d-4e4f328bec4f 34 fields · synced May 30, 2026