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Safecare Vaginal PH Rapid Test Cassette 3 Tests

by Safecare Biotech (Hangzhou) 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 Number06974246462905 UDI-DI Date18 Mar 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  • Withdrawn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
Safecare Vaginal PH Rapid Test Cassette
Generic Name
Vaginal pH screening IVD, kit, rapid colorimetric, clinical
Model / Ref / Catalog
3 Tests, PH-6012
Primary DI / UDI-DI
06974246462905
FDA Product Code
LNW
GMDN Term
Vaginal pH screening IVD, kit, rapid colorimetric, clinical
Device Class
Class I
Regulation Number
862.1550
GUDID distribution status
In Commercial Distribution

Other devices from Safecare Biotech (Hangzhou) Co., Ltd.

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Properties

  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No