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Auvita

EUDAMED

Class III (EU MDR)

Ref SIRSP008010Model Auvita

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

Identity

Trade Name
Auvita EUDAMED
Device Name
Auvita EUDAMED
Model / Reference
Auvita EUDAMED
SIRSP008010 EUDAMED

Identifiers

Primary DI / UDI-DI
08052742101875 EUDAMED
Basic UDI-DI
805274210Auvita3G 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

Auvita 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 6b116380-0f3d-4c49-94c0-b3dd94fd673b 61 fields · synced Oct 6, 2026