7 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
KENGUARD URINARY DRAINAGE BAG W/ANTIREFLUX CHAMBER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
AAP K-WIRE, STEINMANN PIN, CERCLAGE WIRE
FDA 510(k)
FDA Class 2
·Orthopedic
RAPIDO CUT-AWAY CUTTER
FDA 510(k)
FDA Class 2
·Cardiovascular
GLUMA DESENSITIZER POWERGEL
FDA Adverse Event
Injury
·HERAEUS KULZER GMBH·Product code LBH·January 17, 2013
PUMP MMT-722NAS PRDGM INS V2.2 SK EN
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code MDS·December 8, 2010
ACCU-CHEK ® AVIVA COMBO
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code NBW·July 14, 2014
ev3 Pipeline Flex Embolization Device with Shield Technology. Sold OUS. For neurological endovascular use.
FDA Enforcement
Class I
·Terminated·Micro Therapeutics Inc, Dba Ev3 Neurovascular·April 1, 2020