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CONELOG® Esthomic® Abutment

EUDAMED

Class IIb (EU MDR)

Ref C2231.381W

by ALTATEC GmbH

Identity

Trade Name
CONELOG® Esthomic® Abutment EUDAMED
Device Name
CONELOG® Standard abutment EUDAMED
Model / Reference
C2231.381W EUDAMED

Identifiers

Primary DI / UDI-DI
04099797001075 EUDAMED
Basic UDI-DI
40997970001505000000000HL EUDAMED
Secondary DI
E219C2232381W1 EUDAMED
EMDN Code
P01020180 DENTAL IMPLANTS - ACCESSORIES EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

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® Esthomic® 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 9c271fc5-8479-4c5d-a72c-fae13dcea7f4 61 fields · synced May 29, 2026