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Homedics PX-250HCO

by Shenzhen Hexin Zondan Medical Equipment Co., Ltd.

Listed FDA GUDID listing, not in commercial distribution

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 Number06938395500307 UDI-DI Date22 Apr 2026ListedStatusListed GUDID: not 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  • Withdrawn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
Homedics
Generic Name
Pulse oximeter
Model / Reference
PX-250HCO
Primary DI / UDI-DI
06938395500307
FDA Product Code
PGJ
GMDN Term
Pulse oximeter
Device Class
Class II
Regulation Number
870.2700
GUDID distribution status
Not in Commercial Distribution

Other devices from Shenzhen Hexin Zondan Medical Equipment Co., Ltd.

Properties

  • Over-the-Counter
  • Lot / Batch Number
  • Serial Number
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Expiration Date: No