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CERALOG® PEKK Abutment

EUDAMED

Class IIb (EU MDR)

Ref H2234.4580Ref H2231.4580

by ALTATEC GmbH

Identity

Trade Name
CERALOG® PEKK Abutment EUDAMED
Device Name
CERALOG® PEKK abutment EUDAMED
Model / Reference
H2234.4580 EUDAMED
H2231.4580 EUDAMED

Identifiers

Primary DI / UDI-DI
04099797010558 EUDAMED
04099797010534 EUDAMED
Basic UDI-DI
409979700020010000000009G EUDAMED
Secondary DI
E219H223445801 EUDAMED
E219H223145801 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

CERALOG® PEKK 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 (2)

  • EUDAMED 28ce32c3-a0f5-4a02-86bb-30928a8a48a3 61 fields · synced Sep 18, 2026
  • EUDAMED ed6150dc-0b22-4328-930b-e1b6374e2f4d 61 fields · synced May 18, 2026