Skip to content

Neocement

by Bioceramed - Cerâmicos Para Aplicações Médicas, S.A.

Ref CMT20, CMT2, CMT10Model CAPSCement

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05600269575155 Basic UDI-DI Date24 Apr 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  • Withdrawn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
Neocement
Model / Reference
CAPSCement, CMT20, CMT2, CMT10
Primary DI / UDI-DI
05600269575155, 05600870021546, 05600269575148
Basic UDI-DI
B-05600269575155, B-05600870021546, B-05600269575148
EMDN Code
P900402 Resorbable filling and reconstruction devices
Device Class
Class III
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
PT-MF-000002812

Other devices from Bioceramed - Cerâmicos Para Aplicações Médicas, S.A.

See all devices from Bioceramed - Cerâmicos Para Aplicações Médicas, S.A. →

Properties

  • Sterile
  • Implantable
  • Animal Tissues

Other properties (8)

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