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HighLight Plus

EUDAMED

Class I (EU MDR)

Ref 10353Model HighLight

by INVENTIS S.r.l.

Identity

Trade Name
HighLight Plus EUDAMED
Device Name
HighLight EUDAMED
Model / Reference
HighLight EUDAMED
10353 EUDAMED

Identifiers

Primary DI / UDI-DI
08054187380303 EUDAMED
Basic UDI-DI
805418738HL2KQ EUDAMED
EMDN Code
Z12021010 LARYNGOSTROBOSCOPES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

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

HighLight Plus by INVENTIS S.r.l. — Class I — 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

Manufacturer
INVENTIS S.r.l.
EUDAMED SRN
IT-MF-000012495

Sources (1)

  • EUDAMED c2e17ac6-3cc0-4989-b956-c617ce02d6bb 61 fields · synced Jun 18, 2026