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Bernafon

Bernafon AG · Model 116-21-630-10 · UDI-DI 05711584019740

LRB Prescription
10
510(k) clearances
0
Adverse events
0
Recalls
21
Facilities

Description

WIN 322, NO VC KIT L BE

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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.