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Jeashia HS-401F12

by Zhejiang Honsun Medical Technology Co., 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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06972545090331 UDI-DI Date17 Jul 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  • Withdrawn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
Jeashia
Generic Name
Hand-held examination/treatment light
Model / Reference
HS-401F12
Primary DI / UDI-DI
06972545090331
FDA Product Code
FQP
GMDN Term
Hand-held examination/treatment light
Device Class
Class II
Regulation Number
878.4580
GUDID distribution status
In Commercial Distribution

Other devices from Zhejiang Honsun Medical Technology Co., Ltd.

See all devices from Zhejiang Honsun Medical Technology Co., Ltd. →

Properties

  • Premarket Exempt
  • Lot / Batch Number

Other properties (12)

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