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Abutment, M.

by Roott AG EUDAMED

Active European Union

Ref AMModel Abutments M, P

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number76300538AbutmentsMN6 Basic UDI-DIDate22 Sep 2022RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

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.

Specification

EUDAMED

Model / Reference
Abutments M, P, AM
Primary DI / UDI-DI
17630053812734
Basic UDI-DI
76300538AbutmentsMN6
EMDN Code
P01020180 Dental implants - accessories
Device Class
Class IIb
Market of Registration
Poland

Manufacturer details

EUDAMED SRN
CH-MF-000019071
Authorised representative
Roott UAB LT-AR-000002509

Other devices from Roott AG

See all devices from Roott AG →

Properties

  • Implantable
  • Sutures

Other properties (12)

  • Sterile: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No