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MuReva OM™ 1000329

by Mureva Phototherapy, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

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 Number00199874891422 UDI-DI Date8 Jun 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
MuReva OM™
Generic Name
Red-light phototherapy unit, professional
Model / Reference
1000329
Primary DI / UDI-DI
00199874891422
De Novo Number
FDA Product Code
SGQ
GMDN Term
Red-light phototherapy unit, professional
Device Class
Class II
Regulation Number
872.5595
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (DEN240077)

Other devices from Mureva Phototherapy, Inc.

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No