System, x-ray, mobile
FDA product code IZL · Class 2 · 20 devices · 93 reports · 1 deaths reported · 11 devices named in recalls
- Philips MobileDiagnost wDR 2.2Sedecal · System, X-Ray, Mobile3 recalls7 reports
- DRX-Revolution Mobile X-ray SystemCarestream Health, Inc. · System, x-ray, mobile2 recalls12 reports
- Optima XR200amxGE Medical Systems, L.L.C. · System, x-ray, mobile2 recalls1 report
- Optima XR220amxGE Medical Systems, L.L.C. · System, x-ray, mobile2 recalls0 reports
- Optima XR240amxGE Medical Systems, L.L.C. · System, x-ray, mobile2 recalls0 reports
- DRX-Revolution Mobile X-ray SystemCarestream Health, Inc. · System, x-ray, mobile1 recall16 reports
- SEDECAL Soltus 500Sedecal · System, X-Ray, Mobile1 recall4 reports
- Optima XR240amx HD UpgradeGE Medical Systems, L.L.C. · System, x-ray, mobile1 recall0 reports
- MobileDaRt Evolution 503-79999-01Shimadzu Corporation · System, X-Ray, Mobile1 recall0 reports
- FDR AQRO DR-XD 1000Fujifilm Corporation · System, x-ray, mobile1 recall0 reports
- NA GM60A-40SSamsung Electronics Co., Ltd. · System, X-Ray, Mobile1 recall0 reports
- Mobilett Mira Max 10594738Siemens Healthcare GmbH · System, x-ray, mobile17 reports
- Radiography 7000 M 712010Philips Medical Systems DMC GmbH · System, X-Ray, Mobile8 reports
- FDR Go 566-20000-18Shimadzu Corporation · System, X-Ray, Mobile8 reports
- MOBILETT Elara Max 11107444Siemens Healthcare GmbH · System, x-ray, mobile7 reports
- Mobilett XP 01818363Siemens Healthcare GmbH · System, x-ray, mobile5 reports
- AMX NavigateGE Medical Systems, L.L.C. · System, x-ray, mobile2 reports
- Mobilett XP hybrid 01818454Siemens Healthcare GmbH · System, x-ray, mobile2 reports
- FDR Go 503-79888-11Shimadzu Corporation · System, X-Ray, Mobile1 death2 reports
- DX-D 100 5411/050Agfa · System, x-ray, mobile2 reports