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VERDE mezzo 22

EUDAMED

Class I (EU MDR)

Ref VERMEZ22

by Reinecker Vision GmbH

Identity

Trade Name
VERDE mezzo 22 EUDAMED
Device Name
VERDE EUDAMED
Model / Reference
VERMEZ22 EUDAMED

Identifiers

Primary DI / UDI-DI
04255633800664 EUDAMED
Basic UDI-DI
42556338VERDEQ5 EUDAMED
Direct Marketing DI
04255633800664 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

VERDE mezzo 22 by Reinecker Vision GmbH — 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

EUDAMED SRN
DE-MF-000025998

Sources (1)

  • EUDAMED 242b24fc-3c59-421b-9dcb-a1fca2b7611d 61 fields · synced Jun 17, 2026