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CAMLOG® Impression post

EUDAMED

Class I (EU MDR)

Ref KA2154.3840

by ALTATEC GmbH

Identity

Trade Name
CAMLOG® Impression post EUDAMED
Device Name
CAMLOG® Impression post EUDAMED
Model / Reference
KA2154.3840 EUDAMED

Identifiers

Primary DI / UDI-DI
04099797019964 EUDAMED
Basic UDI-DI
40997970006011000000000FK EUDAMED
Secondary DI
+E219KA215438401 EUDAMED
EMDN Code
P01020180 DENTAL IMPLANTS - ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

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

CAMLOG® Impression post by ALTATEC GmbH — Class I — 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 485e8658-e0ba-4a6b-af77-41ee0f3f499d 61 fields · synced May 23, 2026