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Modulith Slc

EUDAMED

Class IIb (EU MDR)

Ref 33000.0001

by Storz Medical Ag

Identity

Trade Name
MODULITH SLC EUDAMED
Device Name
MODULITH SLC EUDAMED
Model / Reference
33000.0001 EUDAMED

Identifiers

Primary DI / UDI-DI
07630039101510 EUDAMED
Basic UDI-DI
76300391ESWL003-QF EUDAMED
Direct Marketing DI
07630039101510 EUDAMED
EMDN Code
Z12160101 EXTRACORPOREAL LITHOTRIPTERS 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

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

Modulith Slc by Storz Medical AG — Class IIb — 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
Storz Medical Ag
EUDAMED SRN
CH-MF-000014374
Authorised Representative
STORZ MEDICAL Deutschland GmbH DE-AR-000009017

Sources (1)

  • EUDAMED f2d81390-4e84-4b42-937f-9adbc15f90e9 61 fields · synced Jul 22, 2026