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Hyalubrix

EUDAMED

Class III (EU MDR)

Ref 10000825Model EQ47-01-1CRef 10000952

by Fidia Farmaceutici S.p.A.

Identity

Trade Name
HYALUBRIX EUDAMED
Device Name
HYALUBRIX EUDAMED
Model / Reference
EQ47-01-1C EUDAMED
10000825 EUDAMED
10000952 EUDAMED

Identifiers

Primary DI / UDI-DI
D-100008253R EUDAMED
D-100009523Z EUDAMED
Basic UDI-DI
B-100008253R EUDAMED
B-100009523Z EUDAMED
EMDN Code
P900402 RESORBABLE FILLING AND RECONSTRUCTION DEVICES EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Germany EUDAMED
Italy 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

Hyalubrix 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 (2)

  • EUDAMED 0fda73de-d774-4908-b169-e5d3a429fd33 61 fields · synced Aug 4, 2026
  • EUDAMED ba28fd30-9152-424c-b4dd-a89bc83aef47 61 fields · synced May 17, 2026