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Nar 80-1662

by North American Rescue, LLC.

Nar 80-1662 is a Class I device made by North American Rescue, LLC., listed in FDA GUDID since 28 Feb 2024 (UDI-DI 00842209130412), registry data as of 22 Oct 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00842209130412 UDI-DI Date28 Feb 2024ListedStatusListed 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  • Withdrawn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
Wound hydrogel dressing, non-antimicrobial
Model / Ref / Catalog
80-1662
Primary DI / UDI-DI
00842209130412
FDA product code
OHO, NAE
GMDN term
Wound hydrogel dressing, non-antimicrobial
Device class
Class I
Regulation number
878.4014, 878.4022
GUDID distribution status
In Commercial Distribution

Related devices

Category: First aid kit, non-medicated, single-useWound hydrogel dressing, non-antimicrobial

Similar devices in this category

Other devices filed under Wound hydrogel dressing, non-antimicrobial.

Other devices from North American Rescue, LLC.

See all devices from North American Rescue, LLC. →

Properties

  • Single use
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)