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S 53-K

BIOTRONIK SE & Co. KG · Model 107235 · UDI-DI 04035479145019

DRB Prescription
1
510(k) clearances
1,275
Adverse events (77 deaths)
0
Recalls
39
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.