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Articulade

EUDAMED

Class III (EU MDR)

Ref SIISP016020Model ArticuladeRef SIISP010050Ref SIISP020025

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

Identity

Trade Name
Articulade EUDAMED
Device Name
Articulade EUDAMED
Model / Reference
Articulade EUDAMED
SIISP016020 EUDAMED
SIISP010050 EUDAMED
SIISP020025 EUDAMED

Identifiers

Primary DI / UDI-DI
08052742101394 EUDAMED
08052742101431 EUDAMED
08052742101370 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

Articulade 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 (3)

  • EUDAMED 964b02c6-ce67-4d17-8109-0a91ef2f7d82 61 fields · synced Oct 6, 2026
  • EUDAMED 9161f6c0-c1b6-4a87-aeb7-5f31a2de5c89 61 fields · synced May 18, 2026
  • EUDAMED 562e4d84-b75e-4b61-bf26-379709507c22 61 fields · synced May 18, 2026