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mezzo Focus 20 KT V5.0

EUDAMED

Class I (EU MDR)

Ref MEZF20X1

by Reinecker Vision GmbH

Identity

Trade Name
mezzo Focus 20 KT V5.0 EUDAMED
Device Name
Bildschirmlesesystem EUDAMED
Model / Reference
MEZF20X1 EUDAMED

Identifiers

Primary DI / UDI-DI
04255633800015 EUDAMED
Basic UDI-DI
42556338BLSVY EUDAMED
Direct Marketing DI
04255633800015 EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

Category: Device sterilization/disinfection container, reusable

mezzo Focus 20 KT V5.0 by Reinecker Vision GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
DE-MF-000025998

Sources (1)

  • EUDAMED cfdbe41b-23bf-4493-863e-a052869e961c 61 fields · synced Jul 21, 2026