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Magnetolith

EUDAMED

Class IIa (EU MDR)

Ref 30500.0001

by Storz Medical Ag

Identity

Trade Name
MAGNETOLITH EUDAMED
Device Name
MAGNETOLITH EUDAMED
Model / Reference
30500.0001 EUDAMED

Identifiers

Primary DI / UDI-DI
07630039101251 EUDAMED
Basic UDI-DI
B-07630039101251 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

Magnetolith by Storz Medical 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

Manufacturer
Storz Medical Ag
EUDAMED SRN
CH-MF-000014374
Authorised Representative
STORZ MEDICAL Deutschland GmbH DE-AR-000009017

Sources (1)

  • EUDAMED d3f5e42c-30c9-4dc5-8f53-dd0a5d77edec 61 fields · synced May 23, 2026