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YaluMOVE®

EUDAMED

Class III (EU MDR)

Ref SIISP010040Model Articulade

by S.A.L.F. S.p.A. Laboratorio Farmacologico

Identity

Trade Name
YaluMOVE® EUDAMED
Device Name
Articulade EUDAMED
Model / Reference
Articulade EUDAMED
SIISP010040 EUDAMED

Identifiers

Primary DI / UDI-DI
08052742101424 EUDAMED
Basic UDI-DI
805274210ArticuZK 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

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

YaluMOVE® by S.A.L.F. S.p.A. Laboratorio Farmacologico — Class III — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
IT-MF-000010720

Sources (1)

  • EUDAMED 05e473ba-d84a-40eb-8bf3-e116c123fad8 61 fields · synced Jun 20, 2026