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Neurolith

EUDAMED

Class IIb (EU MDR)

Ref 31000.0001

by Storz Medical Ag

Identity

Trade Name
NEUROLITH EUDAMED
Device Name
NEUROLITH EUDAMED
Model / Reference
31000.0001 EUDAMED

Identifiers

Primary DI / UDI-DI
07630039100926 EUDAMED
Basic UDI-DI
B-07630039100926 EUDAMED
EMDN Code
Z12101106 NEUROLOGICAL STIMULATORS EUDAMED

Classification

Device Class
Class IIb 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

Neurolith by Storz Medical AG — Class IIb — 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 ff3229ee-3a31-49be-8017-2dabd50466ec 61 fields · synced Aug 3, 2026