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Bleeding Control Kit 04

by Safeguard Us Operating, 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 2 Nov 2026. What this means

Regulatory status

as of registry sync 2 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberM6898723101040 UDI-DI Date22 Oct 2026ListedStatusListed 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  • Withdrawn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
Bleeding Control Kit
Generic Name
First aid kit, non-medicated, single-use
Model / Ref / Catalog
04, 87-231-01
Primary DI / UDI-DI
M6898723101040
FDA Product Code
OHO
GMDN Term
First aid kit, non-medicated, single-use
Device Class
Class I
Regulation Number
878.4014
GUDID distribution status
In Commercial Distribution

Other devices from Safeguard Us Operating, LLC

See all devices from Safeguard Us Operating, LLC →

Properties

  • Single Use
  • Over-the-Counter
  • Convenience Kit
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No