Kit, nephroscope
FDA product code FGA · Class 2 · 12 devices · 172 reports · 6 deaths reported · 1 devices named in recalls
- HALOGEN LIGHT SOURCE OLYMPUS CLK-4Olympus Medical Systems Corp. · Kit, nephroscope61 reports
- MIP Minimal Invasive PCNL 27840KAKarl Storz GmbH & Co. KG · Kit, nephroscope1 recall3 reports
- HALOGEN LIGHT SOURCE CLH-SCOlympus Medical Systems Corp. · Kit, nephroscope37 reports
- Olympus WA33036AOLYMPUS Winter & Ibe GmbH · Kit, Nephroscope27 reports
- Olympus A37025AOLYMPUS Winter & Ibe GmbH · Kit, Nephroscope4 deaths20 reports
- OES CYSTONEPHROFIBERSCOPE OLYMPUS CYF-5AOlympus Medical Systems Corp. · Kit, nephroscope9 reports
- n.a. 27290KKarl Storz GmbH & Co. KG · Kit, nephroscope4 reports
- n.a. 27290MKarl Storz GmbH & Co. KG · Kit, nephroscope4 reports
- Olympus A37022AOLYMPUS Winter & Ibe GmbH · Kit, Nephroscope2 deaths2 reports
- PANOVIEW 8964401Richard Wolf GmbH · Kit, nephroscope2 reports
- PANOVIEW PLUS 8965401Richard Wolf GmbH · Kit, nephroscope2 reports
- PANOVIEW PLUS 8965411Richard Wolf GmbH · Kit, nephroscope1 report