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Duodynator

EUDAMED

Class IIa (EU MDR)

Ref 032-0-2000

by gbo Medizintechnik AG

Identity

Trade Name
Duodynator EUDAMED
Device Name
Duodynator EUDAMED
Model / Reference
032-0-2000 EUDAMED

Identifiers

Primary DI / UDI-DI
04260364810080 EUDAMED
Basic UDI-DI
B-04260364810080 EUDAMED
EMDN Code
Z120601 ELECTROTHERAPY EQUIPMENT (INCLUDED TENS) EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Duodynator by Gbo Medizintechnik Ag — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
DE-MF-000018065

Sources (1)

  • EUDAMED e18c4a82-83aa-4bee-b35d-9f08420aca81 61 fields · synced Jul 9, 2026