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Cartivita

EUDAMED

Class III (EU MDR)

Ref EHA303CAR-GGP

by Erc Bi̇yoteknoloji̇ San.ve Diş Ti̇c.aş.

Identity

Trade Name
CARTIVITA EUDAMED
Model / Reference
EHA303CAR-GGP EUDAMED

Identifiers

Primary DI / UDI-DI
08681665505646 EUDAMED
Basic UDI-DI
B-08681665505646 EUDAMED
EMDN Code
P900402 RESORBABLE FILLING AND RECONSTRUCTION DEVICES EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

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

Cartivita by Erc Bi̇yoteknoloji̇ San.ve Diş Ti̇c.aş. — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
TR-MF-000027082

Sources (1)

  • EUDAMED 1cd3fa9e-fed9-4608-83a5-1e7eaf72171d 61 fields · synced Oct 6, 2026