6 results
·
25ms
·
Sources: EU EUDAMED, US FDA
BAG RESUSCITATOR
FDA 510(k)
FDA Class 2
·Anesthesiology
ACCUTECH ENDOLITE PROBE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
priti multidisc ZrO2 High Translucent
FDA 510(k)
FDA Class 2
·Dental
FLEXI-SEAL CONTROL FMS KIT US
FDA Adverse Event
Injury
·CONVATEC INC·Product code KNT·April 11, 2014
SOFTCLIX LANCET DEVICE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code FMK·July 13, 2007
PENUMBRA SYSTEM ASPIRATION PUMP 110
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code BTA·September 26, 2012