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Medidenta EJ0008-Medi

by Handpiece Parts & Repairs, Inc.

Medidenta EJ0008-Medi is a Class I device made by Handpiece Parts & Repairs, Inc., listed in FDA GUDID since 20 May 2022 (UDI-DI 00810988030377), 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 Number00810988030377 UDI-DI Date20 May 2022ListedStatusListed 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  • Withdrawn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
Medidenta
Generic name
Dental power tool system handpiece, line-powered
Model / Ref / Catalog
EJ0008-MEDI
Primary DI / UDI-DI
00810988030377
FDA product code
EBW
GMDN term
Dental power tool system handpiece, line-powered
Device class
Class I
Regulation number
872.4200
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental power tool system handpiece, line-powered

Similar devices

Other devices filed under FDA product code EBW (Controller, Foot, Handpiece And Cord).

Other devices from Handpiece Parts & Repairs, Inc.

See all devices from Handpiece Parts & Repairs, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Serial number
Other properties (12, all answered No)