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Hymovis

EUDAMED

Class III (EU MDR)

Ref 10001310Model EQC5-01-1DRef 10001205Ref 11000358Model EQC5-01-1C

by Fidia Farmaceutici S.p.A.

Identity

Trade Name
HYMOVIS EUDAMED
Device Name
HYMOVIS EUDAMED
Model / Reference
EQC5-01-1D EUDAMED
10001310 EUDAMED
10001205 EUDAMED
EQC5-01-1C EUDAMED
11000358 EUDAMED

Identifiers

Primary DI / UDI-DI
D-100013102S EUDAMED
D-100012052U EUDAMED
D-110003583Y EUDAMED
Basic UDI-DI
B-100013102S EUDAMED
B-100012052U EUDAMED
B-110003583Y EUDAMED
EMDN Code
P900402 RESORBABLE FILLING AND RECONSTRUCTION DEVICES EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Italy EUDAMED
Germany EUDAMED
Austria EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMEDEUDAMED

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

Hymovis by Fidia Farmaceutici S.p.A. — 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
IT-MF-000026988

Sources (3)

  • EUDAMED 4e82f690-4526-4330-ba63-d1ff7952aa8f 61 fields · synced Jul 13, 2026
  • EUDAMED bf6eb5b9-e9c3-4ed3-8602-fd82696df885 61 fields · synced May 18, 2026
  • EUDAMED 9014e835-6b9b-4084-a476-3b51f07cb998 61 fields · synced May 18, 2026