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Nar 85-4137

by North American Rescue, LLC.

Nar 85-4137 is a Class II device made by North American Rescue, LLC., listed in FDA GUDID since 22 Mar 2023 (UDI-DI 00842209126576), 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 Number00842209126576 UDI-DI Date22 Mar 2023ListedStatusListed 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  • Withdrawn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
Cricothyrotomy kit, single-use
Model / reference
85-4137
Primary DI / UDI-DI
00842209126576
FDA product code
OGP
GMDN term
Cricothyrotomy kit, single-use
Device class
Class II
Regulation number
868.5800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Cricothyrotomy kit, single-use

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)