8 results
·
27ms
·
Sources: EU EUDAMED, US FDA
DERMALAND DURAL HOOKS
FDA 510(k)
FDA Class 1
·Neurology
Ophthalmic Spatula
FDA UDI
KATENA PRODUCTS, INC.·00841668102497·MILDER PHACO SPATULA, LEFT
AC3 Series IABP
FDA 510(k)
FDA Class 2
·Cardiovascular
MARIGEN WOUND DRESSING
FDA 510(k)
FDA Unclassified
·Unknown
400 DENTAL NDL 30SH
FDA Adverse Event
Injury
·COVIDIEN·Product code DZM·October 17, 2019
PLUM A+ DRIVER ED 2
FDA Adverse Event
Malfunction
·HOSPIRACOSTA RICA LTD.·Product code FRN·February 10, 2014
STERIS SYSTEM 1E
FDA Adverse Event
STERIS CORPORATION - HOPKINS·Product code MED·November 14, 2012
FLEXICAP DISCONNECT CAP
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·September 13, 2010