7 results
·
28ms
·
Sources: EU EUDAMED, US FDA
CATHETER, URETHRAL PRESSURE, UPE-10 & 12
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
STORZ SLX-F2 STORM TOUCH
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
INSTRUMENT RACK FOR DAWSON-YUHL INSTR.
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
TI LOW PROFILE SCREW 6.5X30MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LPH·April 24, 2014
CAPIOX FX OXYGENATOR
FDA Adverse Event
Malfunction
·TERUMO CORP.·Product code DTZ·October 1, 2012
STERIS 20 STERILANT
FDA Adverse Event
Injury
·STERIS CORPORATION - HOPKINS·Product code MED·July 27, 2010
TI MATRIXMANDIBLE 6 HOLE PLATE 1.5MM THICK
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code JEY·December 5, 2020