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Jermei JM691

by Shenzhen Jermei Medical Device 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 Number06972433811246 UDI-DI Date10 Jun 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  • Withdrawn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
Jermei
Generic Name
Eyelid heat therapy system control unit
Model / Reference
JM691
Primary DI / UDI-DI
06972433811246
FDA Product Code
ISA
GMDN Term
Eyelid heat therapy system control unit
Device Class
Class I
Regulation Number
890.5660
GUDID distribution status
In Commercial Distribution

Other devices from Shenzhen Jermei Medical Device Technology Co., Ltd

See all devices from Shenzhen Jermei Medical Device Technology Co., Ltd →

Properties

  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Serial Number
  • Manufacturing Date

Other properties (9)

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