Permanent Pacemaker Electrode
Biotronik Se & Co. Kg's record for this product code
MDR events2,109All time
Recalls0All time
510(k) clearances0All time
Recent MDR events
2,109 adverse event reports on file
- SX 53/15 BPJul 14, 2026Injury1028232-2026-03297
- ELOX 45 BPJul 14, 2026Injury1028232-2026-03298
- ELOX 53 BPJun 17, 2026Malfunction1028232-2026-02943
- PERMANENT PACEMAKER ELECTRODEMay 11, 2026MalfunctionMW5188002
- AROX 53-BPMay 5, 2026Malfunction1028232-2026-02150
- AROX 45-JBPMay 4, 2026Malfunction1028232-2026-02146
- PERMANENT PACEMAKER ELECTRODEApr 13, 2026MalfunctionMW5186718
- PERMANENT PACEMAKER ELECTRODEApr 13, 2026MalfunctionMW5186720
- RETROX RX 60-BPMar 23, 2026Malfunction1028232-2026-01433
- RETROX RX 45-JBPMar 23, 2026Malfunction1028232-2026-01432
Recalls
0 recall events for this product code
No recalls on file for Biotronik Se & Co. Kg under this product code.
510(k) clearances
0 clearances for this product code
No 510(k) clearances on file for Biotronik Se & Co. Kg under this product code.