← Back to catalogue

Electromagnetic Stimulator

EUDAMED

Class IIa (EU MDR)

Ref accucurv

by Lutronic Corporation

Identity

Device Name
Electromagnetic Stimulator EUDAMED
Model / Reference
accucurv EUDAMED

Identifiers

Primary DI / UDI-DI
D-11010E3 EUDAMED
Basic UDI-DI
B-11010E3 EUDAMED
EMDN Code
Z120606 MAGNETOTHERAPY EQUIPMENT 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

Electromagnetic Stimulator by Lutronic Corporation — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
KR-MF-000009035
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED e2b90fcd-49ef-4622-87e9-31678ead1c0d 61 fields · synced Jul 10, 2026