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CAMLOG® CAM Titanium Blank

EUDAMED

Class IIb (EU MDR)

Ref K2471.5027

by ALTATEC GmbH

Identity

Trade Name
CAMLOG® CAM Titanium Blank EUDAMED
Device Name
CAMLOG® CAM Titanium Blank EUDAMED
Model / Reference
K2471.5027 EUDAMED

Identifiers

Primary DI / UDI-DI
04099797018271 EUDAMED
Basic UDI-DI
40997970001115000000000DX EUDAMED
Secondary DI
E219K247150271 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

CAMLOG® CAM Titanium Blank 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 f0538e65-e049-4616-828f-04bbd1fed835 61 fields · synced May 23, 2026