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RhodoLED XL BF-LED-XL

by Biofrontera Discovery GmbH

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 2 Nov 2026. What this means

Regulatory status

as of registry sync 2 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04262581550015 UDI-DI Date16 Oct 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  • Withdrawn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
RhodoLED XL
Generic name
Skin photodynamic therapy lamp
Model / reference
BF-LED-XL
Primary DI / UDI-DI
04262581550015
FDA product code
MYH
GMDN term
Skin photodynamic therapy lamp
Device class
Class III
GUDID distribution status
In Commercial Distribution

Other devices from Biofrontera Discovery GmbH

Properties

  • Prescription use
  • Combination product
  • Serial number
  • Manufacturing date

Other properties (11)

  • Supplied sterile: No
  • Sterilise before use: No
  • Single use: No
  • Implantable: No
  • Contains latex: No
  • Over-the-counter: No
  • Convenience kit: No
  • HCT/P: No
  • Premarket exempt: No
  • Lot / batch number: No
  • Expiration date: No