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SenopiMed

EUDAMED

Class I (EU MDR)

Ref SenopiMed

by Senopi Ag

Identity

Trade Name
SenopiMed EUDAMED
Device Name
SenopiMed EUDAMED
Model / Reference
SenopiMed EUDAMED

Identifiers

Primary DI / UDI-DI
07649990898018 EUDAMED
Basic UDI-DI
7649990898SenopiMedYZ EUDAMED
Direct Marketing DI
07649990898018 EUDAMED
EMDN Code
N010299 NEUROLOGIC PHYSIOTHERAPHY DEVICES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Denmark 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

SenopiMed by Senopi Ag — 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
Senopi Ag
EUDAMED SRN
CH-MF-000035610
Authorised Representative
SigmaTech Nordic ApS DK-AR-000039264

Sources (1)

  • EUDAMED 1e586019-168d-46aa-bcf8-6006758daa02 61 fields · synced Jul 9, 2026