Implantable cardioverter defibrillator (non-CRT)
FDA product code LWS · Class 3 · 211 devices · 69,456 reports · 663 deaths reported · 75 devices named in recalls
- Entrant™ CDDRA300TSt. Jude Medical, Inc. · Implantable cardioverter defibrillator (non-CRT)2 reports
- ORIGEN™ EL ICD DR D052Boston Scientific Corporation · Implantable cardioverter defibrillator (non-CRT)1 report
- ORIGEN™ EL ICD VR D050Boston Scientific Corporation · Implantable cardioverter defibrillator (non-CRT)1 report
- Ilesto 7 VR-T DX DF-1 383595BIOTRONIK SE & Co. KG · Implantable cardioverter defibrillator (non-CRT)1 report
- Iforia 7 VR-T 390087BIOTRONIK SE & Co. KG · Implantable cardioverter defibrillator (non-CRT)1 report
- Itrevia 5 VR-T DX 393055BIOTRONIK SE & Co. KG · Implantable cardioverter defibrillator (non-CRT)1 report
- Itrevia 5 VR-T 393059BIOTRONIK SE & Co. KG · Implantable cardioverter defibrillator (non-CRT)1 death1 report
- Ilivia Neo 7 VR-T DX DF-1 ProMRI 429530BIOTRONIK SE & Co. KG · Implantable cardioverter defibrillator (non-CRT)1 report
- Intica Neo 5 VR-T DF-1 ProMRI 429570BIOTRONIK SE & Co. KG · Implantable cardioverter defibrillator (non-CRT)1 report
- Durata™ 7120/75St. Jude Medical, Inc. · Implantable cardioverter defibrillator (non-CRT)1 report
- Durata™ 7122/75St. Jude Medical, Inc. · Implantable cardioverter defibrillator (non-CRT)1 report