9 results
·
18ms
·
Sources: EU EUDAMED, US FDA
IL TEST DIGOXIN & IL TEST DIGOXIN CALIBRATORS
FDA 510(k)
FDA Class 2
·Clinical Toxicology
MYOCARDIAL INSULATOR
FDA 510(k)
FDA Class 2
·Cardiovascular
Paltop Dental Implant System
FDA 510(k)
FDA Class 2
·Dental
HL20 BUBBLE SENSOR
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTQ·January 30, 2015
PLATE
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code HRS·February 5, 2013
FAT EMUL 1.6 CAS CP
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·December 3, 2010
RIATA ACTIVE FIXATION
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·July 18, 2014
BD SAFE-CLIP¿ NEEDLE CLIPPING & STORAGE DEVICE
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMI·September 25, 2019
SHARPS DISPOSAL
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMI·August 16, 2019