Skip to content

Trauma Kit H-9954

by Uline, Inc.

Trauma Kit H-9954 is a device classified as Not classified made by Uline, Inc., listed in FDA GUDID since 6 Apr 2026 (UDI-DI 10850015055826), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10850015055826 UDI-DI Date6 Apr 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  • Withdrawn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
Trauma Kit
Generic name
First aid kit, medicated
Model / reference
H-9954
Primary DI / UDI-DI
10850015055826
FDA product code
LRR
GMDN term
First aid kit, medicated
Device class
N
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code LRR (First Aid Kit With Drug).

Other devices from Uline, Inc.

See all devices from Uline, Inc. →

Properties

  • Single use
  • Over-the-counter
  • Convenience kit
  • Combination product
Other properties (11, all answered No)