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DuoMAG XT

EUDAMED

Class IIa (EU MDR)

Ref 00-133

by DEYMED Diagnostic s.r.o.

Identity

Trade Name
DuoMAG XT EUDAMED
Device Name
DuoMAG EUDAMED
Model / Reference
00-133 EUDAMED

Identifiers

Primary DI / UDI-DI
08592566001338 EUDAMED
Basic UDI-DI
8592566-DM-000018L EUDAMED
Direct Marketing DI
08592566001338 EUDAMED
EMDN Code
Z12101105 MAGNETIC STIMULATORS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Czechia 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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

DuoMAG XT by DEYMED Diagnostic s.r.o. — Class IIa — 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
CZ-MF-000001824

Sources (1)

  • EUDAMED add1d0a9-cb1e-4ab0-8272-dbf577ee328b 61 fields · synced Jun 9, 2026