Skip to content

N/A Fast Response Kit

by Shenzhen WAP-health Technology Co.Ltd

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 Number06975033060076 UDI-DI Date24 Aug 2024ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Generic Name
First aid kit, non-medicated, single-use
Model / Reference
Fast Response Kit
Primary DI / UDI-DI
06975033060076
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

Related devices

Category: First aid kit, non-medicated, single-use

Other devices from Shenzhen WAP-health Technology Co.Ltd

  • Wap 1

    Class I

Properties

  • Sterile
  • Single Use
  • Convenience Kit
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No