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Acteon X-MIND evo 3D

by Dental Xray Company SRL

Listed FDA GUDID listing, not in commercial distribution

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08052870661012 UDI-DI Date1 Jul 2019ListedStatusListed GUDID: not 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  • Withdrawn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
Acteon
Generic Name
Stationary panoramic/tomographic dental x-ray system, digital
Model / Reference
X-MIND evo 3D
Primary DI / UDI-DI
08052870661012
FDA Product Code
MUH
GMDN Term
Stationary panoramic/tomographic dental x-ray system, digital
Device Class
Class II
Regulation Number
872.1800
GUDID distribution status
Not in Commercial Distribution

Properties

  • Prescription Use
  • Serial Number

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No