Skip to content

NAR Kit 30-0013-NB

by North American Rescue, LLC.

NAR Kit 30-0013-NB is a Class II device made by North American Rescue, LLC., listed in FDA GUDID since 16 Nov 2023 (UDI-DI 00842209129256), 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 Number00842209129256 UDI-DI Date16 Nov 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  • Withdrawn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 Kit
Generic name
Peripheral intravenous catheterization kit, non-sensing
Model / Ref / Catalog
30-0013-NB
Primary DI / UDI-DI
00842209129256
FDA product code
LRS
GMDN term
Peripheral intravenous catheterization kit, non-sensing
Device class
Class II
Regulation number
880.5200
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code LRS (I.V. Start Kit).

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)