← Back to catalogue

Oculade

EUDAMED

Class III (EU MDR)

Ref SIOSP010005Model Oculade

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

Identity

Trade Name
Oculade EUDAMED
Device Name
Oculade EUDAMED
Model / Reference
Oculade EUDAMED
SIOSP010005 EUDAMED

Identifiers

Primary DI / UDI-DI
08052742101592 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

Oculade 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
IT-MF-000010720

Sources (1)

  • EUDAMED 8f8c92fa-d91e-4b26-a70e-cbbf55277e28 61 fields · synced Jun 19, 2026