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Intravisc

EUDAMED

Class III (EU MDR)

Ref N/AModel Intravisc

by Caregen Co., Ltd.

Identity

Trade Name
Intravisc EUDAMED
Device Name
Intra-articular Filler EUDAMED
Model / Reference
Intravisc EUDAMED
N/A EUDAMED

Identifiers

Primary DI / UDI-DI
08809171380018 EUDAMED
Basic UDI-DI
B-08809171380018 EUDAMED
EMDN Code
P900402 RESORBABLE FILLING AND RECONSTRUCTION DEVICES EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Denmark EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Intravisc by Caregen Co., Ltd. — 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

Manufacturer
Caregen Co., Ltd.
EUDAMED SRN
KR-MF-000009948
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED ab192e34-4c5c-4863-b8c1-6a6ba2e57fe7 61 fields · synced Jun 18, 2026