8 results
·
19ms
·
Sources: EU EUDAMED, US FDA
COWBOY X
FDA 510(k)
FDA Class 2
·Cardiovascular
TITERTEK TWINREADER 78-630-00
FDA 510(k)
FDA Class 1
·Clinical Chemistry
DYNATECH MR4000 MICROPLATE READER
FDA 510(k)
FDA Class 1
·Clinical Chemistry
FRESENIUS DIALYSIS DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·FRESENIUS MEDICAL CARE-NORTH AMERICA·Product code KDI·May 16, 2008
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code OYC·February 5, 2013
VITALITY 2
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 3, 2011
MARYLAND BIPOLAR FORCEPS INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·July 18, 2014
KLS Martin Cranial Implants - MR Conditional; K944565: KLS-Martin Micro Osteosynthesis System (1.5MM); K971297: KLS Martin Centre-Drive Drill-Free Screw; K060177: KLS Martin Rigid Fixation - Sterile; K062570: Individual Patient Solutions - Ti (IPS-Ti); K072707: Individual Patient Solutions - PEEK (IPS-PEEK) ; K151382: Individual Patient Solutions - (IPS-PEEK) - STERILE
FDA 510(k)
FDA Class 2
·Neurology