Interventional Fluoroscopic X-ray System
Siemens Healthineers Ag's record for this product code
MDR events293All time
Recalls0All time
510(k) clearances0All time
Recent MDR events
293 adverse event reports on file
- ARTIS ICONO BIPLANEJul 17, 2026Malfunction3004977335-2026-00122
- ARTIS ZEE CEILINGJul 6, 2026Malfunction3004977335-2026-00118
- ARTIS ZEE III FLOORJun 26, 2026Malfunction3004977335-2026-00115
- ARTIS ICONO BIPLANEJun 26, 2026Injury3004977335-2026-00116
- LUMINOS AGILE MAXJun 25, 2026Malfunction3004977335-2026-00114
- ARTIS PHENOJun 23, 2026Malfunction3004977335-2026-00112
- ARTIS ZEE FLOORJun 19, 2026Malfunction3004977335-2026-00109
- ARTIS ICONO BIPLANEJun 16, 2026Malfunction3004977335-2026-00104
- ARTIS ICONO BIPLANEJun 12, 2026Malfunction3004977335-2026-00100
- ARTIS ICONO CEILINGJun 12, 2026Malfunction3004977335-2026-00101
Recalls
0 recall events for this product code
No recalls on file for Siemens Healthineers Ag under this product code.
510(k) clearances
0 clearances for this product code
No 510(k) clearances on file for Siemens Healthineers Ag under this product code.