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Tomtar Gs

EUDAMED

Class I (EU MDR)

Ref 200330

by DIETZ GmbH

Identity

Device Name
TOMTAR GS EUDAMED
Model / Reference
200330 EUDAMED

Identifiers

Primary DI / UDI-DI
04260644771247 EUDAMED
Basic UDI-DI
42602416846GHS000018C EUDAMED
Direct Marketing DI
04260644771247 EUDAMED
EMDN Code
Y120603 WALKING FRAMES, 4 TIPS 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

Tomtar Gs by DIETZ 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

Manufacturer
DIETZ GmbH
EUDAMED SRN
DE-MF-000009121

Sources (1)

  • EUDAMED be685eba-cb59-49ad-b30a-ba3c34e68202 61 fields · synced Jun 18, 2026