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callington 4852/KIT/PPE

by Firstar Healthcare Company Limited (Guangzhou)

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB4484852KITPPE0 UDI-DI Date25 Sep 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  • Withdrawn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
callington
Generic Name
First aid kit, non-medicated, single-use
Model / Reference
4852/KIT/PPE
Primary DI / UDI-DI
B4484852KITPPE0
GMDN Term
First aid kit, non-medicated, single-use
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Safe

Other devices from Firstar Healthcare Company Limited (Guangzhou)

See all devices from Firstar Healthcare Company Limited (Guangzhou) →

Properties

  • Single Use
  • Contains Latex
  • Convenience Kit
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

  • Sterile: No
  • Implantable: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No