107 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·CHILLI COOLED ABLATION SYSTEM
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·CHILLI COOLED ABLATION SYSTEM
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·CHILLI COOLED RPM CATHETER
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·CHILLI AND CHILLI RPM COOLED ABLATION SYSTEM
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·CHILLI COOLED ABLATION SYSTEMS
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·CHILLI AND CHILLI RPM COOLED ABLATION SYSTEM
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·CHILLI COOLED ABLATION SYSTEM
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·CHILLI COOLED ABLATION SYSTEM
Catheter, Percutaneous (Valvuloplasty)
FDA Pre-Market Approval
FDA Class 3
·INOUE BALLOON CATHETER
Catheter, Percutaneous (Valvuloplasty)
FDA Pre-Market Approval
FDA Class 3
·INOUE BALLOON CATHETER
Accessories, Soft Lens Products
FDA Pre-Market Approval
FDA Class 2
·THE BOSTON TM CLEANER II
Catheter, Percutaneous (Valvuloplasty)
FDA Pre-Market Approval
FDA Class 3
·Inoue Balloon Catheter
Catheter, Percutaneous (Valvuloplasty)
FDA Pre-Market Approval
FDA Class 3
·TORAY INOUE BALLON CATHETER
Catheter, Percutaneous (Valvuloplasty)
FDA Pre-Market Approval
FDA Class 3
·Inoue-Balloon Catheter
Catheter, Percutaneous (Valvuloplasty)
FDA Pre-Market Approval
FDA Class 3
·TORAY INOUE BALLOON CATHETER
Catheter, Percutaneous (Valvuloplasty)
FDA Pre-Market Approval
FDA Class 3
·Toray Inoue Balloon Catheter
Catheter, Percutaneous (Valvuloplasty)
FDA Pre-Market Approval
FDA Class 3
·INOUE-BALLOON Catheter
Catheter, Percutaneous (Valvuloplasty)
FDA Pre-Market Approval
FDA Class 3
·INOUE BALLOON CATHETER
Catheter, Percutaneous (Valvuloplasty)
FDA Pre-Market Approval
FDA Class 3
·INOUE BALLOON CATHETER
TARGET DEVICE GAMMA3 300X160MM
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS-KIEL·Product code LXH·March 5, 2013