8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
AMICON DIAFILTERS 20 & 30 HEMOFILTERS
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
COBRA BIPOLAR CLAMP, MODEL 15902
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
HEMOCONCENTRATOR
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
HEMOCONCENTRATOR BC 20 PLUS
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code KDI·April 1, 2016
STENOSCOP
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 20, 2014
ASR XL TAP SLV ADAP 12/14+8
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·November 7, 2012
HEARTSTART MRX
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE·Product code MKJ·August 28, 2010
Promote Quadra, Sterile EO, Model # / Part #: CD3221-36/100025054, 60019195; CD3223-36P/100013763; CD3239-40/100029115, 100029254, 100037181; CD3239-40Q/100029116, 100029244, 100037115
FDA Enforcement
Class II
·Terminated·St Jude Medical Inc.·July 4, 2018