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Cempadic®

by implantcast GmbH 33 variants

Ref 02980842Model CEMP20ECOSTINST

Active European Union

CE MDR

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/MDR Number4048844CEMP20ECOSTINSTNS Basic UDI-DI 04048844132378UDI-DIDate30 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

EstoniaLithuaniaGermanyPolandCzech RepublicAustriaGreece
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

  • Austria
  • Czechia
  • Estonia
  • Germany
  • Greece
  • Lithuania
  • Poland

Specification

EUDAMED

Model / Reference
CEMP20ECOSTINST, 02980842
Primary DI / UDI-DI
04048844132378
Basic UDI-DI
4048844CEMP20ECOSTINSTNS
Direct Marketing DI
04048844132378
EMDN Code
L091105 Cementation instruments, reusable
Device Class
Class I
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
DE-MF-000010002

Other devices from implantcast GmbH

See all devices from implantcast GmbH →

Properties

  • Reusable
  • CMR Substance

Other properties (11)

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