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MODULITH®

Storz Medical AG · Model SLX-F2 · UDI-DI 07630039101459

LNS Prescription
2
510(k) clearances
811
Adverse events (30 deaths)
1
Recalls
18
Facilities

Description

Equipment for the extracorporeal induced shock wave therapy for stationary and mobile use.

Recalls

DateFirmReason
2015-09-24Siemens Medical Solutions USA, IncDisplay freeze of MODULARIS hand control results in information not being updated on the display. Current treatment data is not shown to the user.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.