← Back to catalogue

topolino flex 2K V3.1

EUDAMED

Class I (EU MDR)

Ref TOFL2K31

by Reinecker Vision GmbH

Identity

Trade Name
topolino flex 2K V3.1 EUDAMED
Device Name
Kamerasysteme EUDAMED
Model / Reference
TOFL2K31 EUDAMED

Identifiers

Primary DI / UDI-DI
04255633800602 EUDAMED
Basic UDI-DI
42556338CAMUQ EUDAMED
Direct Marketing DI
04255633800602 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

topolino flex 2K V3.1 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
DE-MF-000025998

Sources (1)

  • EUDAMED 9903322b-23ba-4a8d-96d3-5d60237e90ec 61 fields · synced Jul 9, 2026