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Feminine Screening Kit F-1-VO-CVS02

by Savyon Diagnostics Ltd 2 variants

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 Number17290006558937 UDI-DI Date22 Feb 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  • Withdrawn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
Feminine Screening Kit
Generic Name
Vaginal pH screening IVD, kit, rapid colorimetric, clinical
Model / Reference
F-1-VO-CVS02
Primary DI / UDI-DI
17290006558937
FDA Product Code
CEN
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 Savyon Diagnostics Ltd

See all devices from Savyon Diagnostics Ltd →

Properties

  • Single Use
  • Over-the-Counter
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

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