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Modulith Slk

EUDAMED

Class IIb (EU MDR)

Ref 30000.0001Ref 27000.0001Ref 27000

by Storz Medical Ag

Identity

Trade Name
MODULITH SLK EUDAMED
Device Name
MODULITH SLK EUDAMED
Model / Reference
30000.0001 EUDAMED
27000.0001 EUDAMED
27000 EUDAMED

Identifiers

Primary DI / UDI-DI
07630039101497 EUDAMED
07630039101503 EUDAMED
07630039100766 EUDAMED
Basic UDI-DI
76300391ESWL001-Q9 EUDAMED
B-07630039100766 EUDAMED
Direct Marketing DI
07630039101497 EUDAMED
07630039101503 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 Slk by Storz Medical AG — Class IIb — MDD, MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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 (3)

  • EUDAMED cc8a5d46-a8d6-439f-9dbb-f659619e2091 61 fields · synced Oct 6, 2026
  • EUDAMED 59e738b4-16f4-465b-8484-01c902ed2e40 61 fields · synced May 16, 2026
  • EUDAMED f4696d7a-ce62-4261-b423-417d476b21c6 61 fields · synced May 17, 2026