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Replasyn

EUDAMED

Class III (EU MDR)

Ref 10000298Model EQ0301_1A

by Fidia Farmaceutici S.p.A.

Identity

Trade Name
REPLASYN EUDAMED
Device Name
REPLASYN EUDAMED
Model / Reference
EQ0301_1A EUDAMED
10000298 EUDAMED

Identifiers

Primary DI / UDI-DI
D-100002983N EUDAMED
Basic UDI-DI
B-100002983N EUDAMED
EMDN Code
P900402 RESORBABLE FILLING AND RECONSTRUCTION DEVICES EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
France 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

Replasyn 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 (1)

  • EUDAMED ddb1315e-b00b-4731-99e7-8ec844a425ea 61 fields · synced Jun 19, 2026