7 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
InTRAkit
FDA 510(k)
FDA Class 2
·Cardiovascular
KERRISON PUNCH RONGEUR
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896018228·KERRISON PUNCH RONGEUR UP-ANGLE TIP
VERESS CANNULA AND MODULAR VERESS CANNULA
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
POWDER FREE VINYL PATIENT EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
OMNIPOD INSULIN PUMP
FDA Adverse Event
Injury
·INSULET CORPORATION·Product code LZG·May 30, 2013
EON MINI RECHARGEABLE IPG
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 12, 2011
TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC·Product code NIQ·September 16, 2008