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Videomatic 22 F

EUDAMED

Class I (EU MDR)

Ref VIDEO221F

by Reinecker Vision GmbH

Identity

Trade Name
Videomatic 22 F EUDAMED
Device Name
Bildschirmlesesystem EUDAMED
Model / Reference
VIDEO221F EUDAMED

Identifiers

Primary DI / UDI-DI
04255633800770 EUDAMED
Basic UDI-DI
42556338BLSVY EUDAMED
Direct Marketing DI
04255633800770 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

Videomatic 22 F 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 59dbdfef-6167-4b2b-b5f0-da40a2757ee9 61 fields · synced Jul 27, 2026