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Nar 85-5238

by North American Rescue, LLC.

Nar 85-5238 is a Class I device made by North American Rescue, LLC., listed in FDA GUDID since 27 Oct 2026 (UDI-DI 00842209140619), registry data as of 9 Nov 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00842209140619 UDI-DI Date27 Oct 2026ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Nar
Generic name
First aid kit, non-medicated, single-use
Model / Ref / Catalog
85-5238
Primary DI / UDI-DI
00842209140619
FDA product code
OHO
GMDN term
First aid kit, non-medicated, single-use
Device class
Class I
Regulation number
878.4014
GUDID distribution status
In Commercial Distribution

Other devices from North American Rescue, LLC.

See all devices from North American Rescue, LLC. →

Properties

  • Single use
  • Over-the-counter
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)