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Piezomed Pro Accessory 30502002

by W&H Dentalwerk Burmoos

Piezomed Pro Accessory 30502002 is a Class II device made by W&H Dentalwerk Burmoos, listed in FDA GUDID since 8 Jul 2025 (UDI-DI J021305020021), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberJ021305020021 UDI-DI Date8 Jul 2025ListedStatusListed 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  • Withdrawn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
Piezomed Pro Accessory
Generic name
Hard/soft-tissue ultrasonic surgical system
Model / reference
30502002
Primary DI / UDI-DI
J021305020021
FDA product code
ERL, DZI, JDX, HWE
GMDN term
Hard/soft-tissue ultrasonic surgical system
Device class
Class II
Regulation number
874.4250, 872.4120, 888.4580, 878.4820
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Hard/soft-tissue ultrasonic surgical system

Similar devices in this category

Other devices filed under Hard/soft-tissue ultrasonic surgical system.

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Properties

  • Sterilise before use
  • Single use
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)