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Transfer, L, K.

by Roott AG EUDAMED

Active European Union

Ref TOKL

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number76300538TransfersK4A Basic UDI-DIDate21 Oct 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Device Name
Transfer
Model / Reference
TOKL
Primary DI / UDI-DI
17630053806702
Basic UDI-DI
76300538TransfersK4A
Unit of Use DI
07630053806705
EMDN Code
P01020180 Dental implants - accessories
Device Class
Class I
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

Other properties (13)

  • Sterile: No
  • Implantable: 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