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directSTIM Patient Programmer Charger kit

EUDAMED

Class AIMDD (EU MDR)

Ref 12400Model 12300

by Aleva Neurotherapeutics SA

Identity

Trade Name
directSTIM Patient Programmer Charger kit EUDAMED
Device Name
directSTIM Patient Programmer Charger kit EUDAMED
Model / Reference
12300 EUDAMED
12400 EUDAMED

Identifiers

Primary DI / UDI-DI
07640183760051 EUDAMED
Basic UDI-DI
B-07640183760051 EUDAMED
EMDN Code
J020701 NEUROSTIMULATORS PROGRAMMERS EUDAMED

Classification

Device Class
Class AIMDD EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

Yes

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

directSTIM Patient Programmer Charger kit by Aleva Neurotherapeutics SA — Class AIMDD — 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
CH-MF-000015804
Authorised Representative
Veranex Germany GmbH DE-AR-000005578

Sources (1)

  • EUDAMED d2d3762f-574e-42f2-943f-4422a151bf28 61 fields · synced Jun 18, 2026