Electrode, Electrosurgical, Active, Urological
Karl Storz Endoscopy-america, Inc.'s record for this product code
MDR events25All time
Recalls0All time
510(k) clearances1All time
Recent MDR events
25 adverse event reports on file
- N.A.Aug 1, 2025Malfunction22685831
- ENDOSCOPIC ELECTROSURGICAL ELECTRODE, BIPOLARApr 28, 2025Malfunction9610617-2025-00714
- ENDOSCOPIC ELECTROSURGICAL ELECTRODE, BIPOLARApr 28, 2025Malfunction9610617-2025-00715
- ENDOSCOPIC ELECTROSURGICAL ELECTRODE, BIPOLARApr 28, 2025Malfunction9610617-2025-00713
- ENDOSCOPIC ELECTROSURGICAL ELECTRODE, BIPOLARFeb 20, 2025Malfunction9610617-2025-00271
- ENDOSCOPIC ELECTROSURGICAL ELECTRODE, BIPOLARFeb 20, 2025Malfunction9610617-2025-00255
- ENDOSCOPIC ELECTROSURGICAL ELECTRODE, BIPOLARFeb 20, 2025Malfunction9610617-2025-00261
- ENDOSCOPIC ELECTROSURGICAL ELECTRODE, BIPOLARFeb 19, 2025Injury2020550-2025-00254
- ENDOSCOPIC ELECTROSURGICAL ELECTRODE, BIPOLARFeb 19, 2025Injury9610617-2025-00254
- ENDOSCOPIC ELECTROSURGICAL ELECTRODE, BIPOLARDec 5, 2024Malfunction9610617-2024-00494
Recalls
0 recall events for this product code
No recalls on file for Karl Storz Endoscopy-america, Inc. under this product code.
510(k) clearances
1 clearances for this product code