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PowerLaser Basic500 VET Platinum 30054

by Powermedic ApS

PowerLaser Basic500 VET Platinum 30054 is a musculoskeletal/physical therapy laser (FDA Class II; FDA product code ILY, Lamp, Infrared, Therapeutic Heating) made by Powermedic ApS, listed in FDA GUDID since 13 Sep 2023 (UDI-DI 05713592300544), registry data as of 22 Oct 2026.

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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05713592300544 UDI-DI Date13 Sep 2023ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
PowerLaser Basic500 VET Platinum
Generic name
Musculoskeletal/physical therapy laser, home-use
Model / reference
30054
Primary DI / UDI-DI
05713592300544
FDA product code
ILY
GMDN term
Musculoskeletal/physical therapy laser, home-use
Device class
Class II
Regulation number
890.5500
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code ILY (Lamp, Infrared, Therapeutic Heating).

Other devices from Powermedic ApS

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Properties

  • Over-the-counter
  • Serial number
Other properties (13, all answered No)