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by Dentis Co., Ltd EUDAMED

Active European Union

Ref DSLAMCSP451047SModel DENTIS Implant Surgical Instrument System

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number88061691DENTIS-I7L Basic UDI-DIDate27 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • 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
DENTIS Implant Surgical Instrument System
Model / Reference
DENTIS Implant Surgical Instrument System, DSLAMCSP451047S
Primary DI / UDI-DI
08800053091886
Basic UDI-DI
88061691DENTIS-I7L
EMDN Code
P01020180 Dental implants - accessories
Device Class
Class I
Market of Registration
Spain

Manufacturer details

EUDAMED SRN
KR-MF-000012523
Authorised representative
BEST FIT IMPLANTS S.A. ES-AR-000048728

Other devices from Dentis Co., Ltd.

See all devices from Dentis Co., Ltd. →

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