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Hyal System Acp

EUDAMED

Class III (EU MDR)

Ref 10001263Model QQE2-00-1A1

by Fidia Farmaceutici S.p.A.

Identity

Trade Name
HYAL SYSTEM ACP EUDAMED
Device Name
HYAL SYSTEM ACP EUDAMED
Model / Reference
QQE2-00-1A1 EUDAMED
10001263 EUDAMED

Identifiers

Primary DI / UDI-DI
D-100012633A EUDAMED
Basic UDI-DI
B-100012633A EUDAMED
EMDN Code
P900402 RESORBABLE FILLING AND RECONSTRUCTION DEVICES EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
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

Hyal System Acp 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 51254d72-d4c2-4fab-9e0d-478ab116f582 61 fields · synced Sep 18, 2026