8 results
·
24ms
·
Sources: EU EUDAMED, US FDA
OLBERT CATHETER SYS FOR URETERAL DILATION
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
XENO ADHESIVE WITH ACTIVATOR
FDA 510(k)
FDA Class 2
·Dental
Hansen Medical Magellan Robotic Catheter 6Fr and Accessory Components
FDA 510(k)
FDA Class 2
·Cardiovascular
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·June 5, 2014
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·November 29, 2012
STARCLOSE SE VASCULAR CLOSURE SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR - VASCULAR SOLUTIONS·Product code MGB·September 29, 2010
ASR ACETABULAR IMPLANT 50
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·October 2, 2018
TOTAL ASR FEM IMP SIZE 45
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·October 2, 2018