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CONELOG® Multi-unit Abutment

EUDAMED

Class IIb (EU MDR)

Ref C2264.5010

by ALTATEC GmbH

Identity

Trade Name
CONELOG® Multi-unit Abutment EUDAMED
Device Name
CONELOG® Bar abutment EUDAMED
Model / Reference
C2264.5010 EUDAMED

Identifiers

Primary DI / UDI-DI
04099797993707 EUDAMED
Basic UDI-DI
40997970001501000000000DY EUDAMED
Secondary DI
E219C226450101 EUDAMED
EMDN Code
P01020180 DENTAL IMPLANTS - ACCESSORIES EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Sutures

Yes

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

CONELOG® Multi-unit Abutment by ALTATEC GmbH — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
ALTATEC GmbH
EUDAMED SRN
DE-MF-000006230

Sources (1)

  • EUDAMED 7c7347c2-02cc-408e-b301-5d5af0229323 61 fields · synced Jun 19, 2026