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QuasarMD TN2507

by Ningbo Jinhui Photoelectricity 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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06977782490029 UDI-DI Date22 Aug 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  • Withdrawn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
QuasarMD
Generic Name
Blue/red/infrared phototherapy lamp
Model / Reference
TN2507
Primary DI / UDI-DI
06977782490029
FDA Product Code
ILO, ILY
GMDN Term
Blue/red/infrared phototherapy lamp
Device Class
Class II
Regulation Number
890.5720, 890.5500
GUDID distribution status
In Commercial Distribution

Other devices from Ningbo Jinhui Photoelectricity Technology Co., Ltd

Properties

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

Other properties (10)

  • 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
  • Expiration Date: No