8 results
·
22ms
·
Sources: EU EUDAMED, US FDA
AMBU SPUR NEONATE
FDA 510(k)
FDA Class 2
·Anesthesiology
HEALTH ESSENTIALS FANCY PERSONAL MASSAGER
FDA 510(k)
FDA Class 1
·Physical Medicine
FLUOROVISION CONTRAST ENHANCER
FDA 510(k)
FDA Class 2
·Radiology
STAINLESS STEEL GREENFIELD VENA CAVA FILTER WITH 12F/4.0MM INTRODUCER SYSTEM
FDA Adverse Event
Death
·BOSTON SCIENTIFIC - CORK·Product code DTK·May 14, 2013
UNKNOWN PRODUCT - SET SCREW
FDA Adverse Event
Injury
·STRYKER OSTEOSYNTHESIS KIEL·Product code HWC·October 12, 2012
PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE
FDA Adverse Event
Injury
·MPRI·Product code LWP·February 15, 2013
PRECISION TEST STRIPS
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 20, 2011
SMALL BATTERY DRIVE
FDA Adverse Event
Malfunction
·SYNTHES OBERDORF·Product code HWE·July 29, 2014