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Abutment

by D.A.N.D Metal Industries North 37 variants

Ref STAA 25 RPModel Angular Abutment Conical 25 RP

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-07290111512803 Basic UDI-DI 07290111512803UDI-DIDate8 Jun 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  • Withdrawn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
Staa 25 Rp
Model / Reference
Angular Abutment Conical 25 RP, STAA 25 RP
Primary DI / UDI-DI
07290111512803
Basic UDI-DI
B-07290111512803
EMDN Code
P010299 Odontological prostheses - other
Device Class
Class IIb
EU market of registration
Romania

Manufacturer details

EUDAMED SRN
IL-MF-000038021
Authorised representative
Obelis s.a. BE-AR-000000106

Related devices

Category: Dental implant suprastructure, permanent, preformed

Other devices from D.A.N.D. Metal Industries North, Ltd.

See all devices from D.A.N.D. Metal Industries North, Ltd. →

Properties

  • Reprocessed

Other properties (10)

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