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Condrodol

EUDAMED

Class I (EU MDR)

Ref 800_546

by Fysioline Oy

Identity

Trade Name
Condrodol EUDAMED
Device Name
Condrodol EUDAMED
Model / Reference
800_546 EUDAMED

Identifiers

Primary DI / UDI-DI
D-84353737087347J EUDAMED
Basic UDI-DI
B-84353737087347J EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Condrodol by Fysioline Oy — Class I — 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
Fysioline Oy
EUDAMED SRN
FI-MF-000001173

Sources (1)

  • EUDAMED 3741af6c-dee9-448c-b214-ba8d0da9cab6 61 fields · synced Aug 1, 2026