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Angled Abutment Screw Wide Plat. - Ext. Hex.

by A. S. Technology Componentes Especiais LTDA.

Ref 201113Model HE ABUTMENT SCREW

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-07908424001135 Basic UDI-DI 07908424001135UDI-DIDate21 Oct 2026RegisteredStatusActive

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  • Withdrawn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 Active

Specification

EUDAMED

Device Name
Dental Components
Model / Reference
HE ABUTMENT SCREW, 201113
Primary DI / UDI-DI
07908424001135
Basic UDI-DI
B-07908424001135
EMDN Code
P01020180 Dental implants - accessories
Device Class
Class IIb
EU market of registration
Portugal

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

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Reusable: 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