8 results
·
20ms
·
Sources: EU EUDAMED, US FDA
CURIS II RF Generator (REF 360100-05)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Sniper Spine System
FDA 510(k)
FDA Class 2
·Orthopedic
ULTRAPACS
FDA 510(k)
FDA Class 2
·Radiology
BD VACUTAINER® K2E 5.4MG PLUS BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·April 26, 2018
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·November 14, 2014
UTERINE MANIPULATOR - 7CM
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code LKF·September 16, 2011
OMNIPOD INSULIN PUMP
FDA Adverse Event
Injury
·INSULET CORPORATION·Product code LZG·July 18, 2013
BD VACUTAINER® K2E 5.4MG PLUS BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·June 1, 2018