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Twist Drill 3.0 Mm

by A. S. Technology Componentes Especiais LTDA.

Ref HD 3.0Model TWIST DRILL

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDD, withdrawn

Ended

Withdrawn

Date not published (CE MDD)

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-07908424006864 Basic UDI-DI 07908424006864UDI-DIDate8 Jun 2026RegisteredStatusWithdrawn No longer placed on the EU market

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Withdrawn

Specification

EUDAMED

Device Name
Instruments
Model / Reference
TWIST DRILL, HD 3.0
Primary DI / UDI-DI
07908424006864
Basic UDI-DI
B-07908424006864
EMDN Code
Z12110102 Dental drills
Device Class
Class IIa

Manufacturer details

EUDAMED SRN
BR-MF-000011065
Authorised representative
Eurofix - Implantes e Componentes Dentários, Lda. PT-AR-000005254

Other devices from A. S. Technology Componentes Especiais LTDA.

See all devices from A. S. Technology Componentes Especiais LTDA. →

Properties

  • Reusable

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No