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BrightCare SQ1221

by The Gilbert Group LLC

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00856614007870 UDI-DI Date2 Dec 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
BrightCare
Generic Name
First aid kit, medicated
Model / Reference
SQ1221
Primary DI / UDI-DI
00856614007870
FDA Product Code
LRR, OHO
GMDN Term
First aid kit, medicated
Device Class
N
Regulation Number
878.4014
GUDID distribution status
In Commercial Distribution

Other devices from The Gilbert Group LLC

See all devices from The Gilbert Group LLC →

Properties

  • Single Use
  • Convenience Kit

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No