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YaluVISTA®

EUDAMED

Class III (EU MDR)

Ref SIOSV010010Model Oculade

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

Identity

Trade Name
YaluVISTA® EUDAMED
Device Name
Oculade EUDAMED
Model / Reference
Oculade EUDAMED
SIOSV010010 EUDAMED

Identifiers

Primary DI / UDI-DI
08052742101684 EUDAMED
Basic UDI-DI
805274210OculadZJ EUDAMED
EMDN Code
Q02030301 OPHTHALMOLOGY, HYALURONIC ACID AND DERIVATIVES 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

YaluVISTA® 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 65cd3c1e-9f75-4213-9044-d508d7bae759 61 fields · synced Jun 19, 2026