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NovoTAL flex

Novocure GmbH · Model SW000128 · UDI-DI 07290107984447

NZK
0
510(k) clearances
790
Adverse events (27 deaths)
0
Recalls
8
Facilities

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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.