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Pro Med by Jouvalle J900

by Omm Imports Inc.

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 Number00850001456791 UDI-DI Date2 May 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  • Withdrawn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
Pro Med by Jouvalle
Generic Name
Blue/red/infrared phototherapy lamp
Model / Reference
J900
Primary DI / UDI-DI
00850001456791
FDA Product Code
OHS, ILY
GMDN Term
Blue/red/infrared phototherapy lamp
Device Class
Class II
Regulation Number
878.4810, 890.5500
GUDID distribution status
In Commercial Distribution

Other devices from Omm Imports Inc.

See all devices from Omm Imports Inc. →

Properties

  • Over-the-Counter
  • Serial Number
  • Manufacturing Date

Other properties (11)

  • 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
  • Lot / Batch Number: No
  • Expiration Date: No