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Titanium cap

EUDAMED

Class IIa (EU MDR)

Ref J2259.6022

by ALTATEC GmbH

Identity

Trade Name
Titanium cap EUDAMED
Device Name
Prosthetic Parts EUDAMED
Model / Reference
J2259.6022 EUDAMED

Identifiers

Primary DI / UDI-DI
04099797010947 EUDAMED
Basic UDI-DI
40997970004502000000000JQ EUDAMED
Secondary DI
E219J225960221 EUDAMED
EMDN Code
P01020180 DENTAL IMPLANTS - ACCESSORIES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

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

Titanium cap by ALTATEC GmbH — Class IIa — 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 04f76219-afa6-43b0-9e3b-fd96300545d2 61 fields · synced May 23, 2026