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Nar 85-1297

by North American Rescue, LLC.

Nar 85-1297 is a Class I device made by North American Rescue, LLC., listed in FDA GUDID since 8 Dec 2022 (UDI-DI 00842209122691), 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 Number00842209122691 UDI-DI Date8 Dec 2022ListedStatusListed 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  • Withdrawn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
Arterial tourniquet, manual, single-use
Model / reference
85-1297
Primary DI / UDI-DI
00842209122691
FDA product code
GAX
GMDN term
Arterial tourniquet, manual, single-use
Device class
Class I
Regulation number
878.5900
GUDID distribution status
In Commercial Distribution

Related devices

Category: Venous tourniquet, single-use

Similar devices

Other devices filed under FDA product code GAX (Tourniquet, Nonpneumatic).

Other devices from North American Rescue, LLC.

See all devices from North American Rescue, LLC. →

Properties

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