8 results
·
19ms
·
Sources: EU EUDAMED, US FDA
MEDFLATOR INFLATION SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756389273·LAPAROSCOPY PACK
VERSAJET II HYDROSURGERY SYSTEM CONSOLE / EXACT HANDPIECES / PLUS HANDPIECES, VERSAJET FOOTSWITCH
FDA 510(k)
FDA Class 2
·General Hospital
FISTULOK FISTULA NEEDLE PROTECTION
FDA 510(k)
FDA Class 2
·General Hospital
PINNACLE SECTOR II CUP 52MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code KWA·January 11, 2013
HAKIM PROGRAMMABLE VALVE WITH PRECHAMBER
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC., MEDOS S.A.·Product code JXG·November 23, 2010
ULTRACISION HARMONIC ACE
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·July 2, 2014
REVERSE SHOULDER SYSTEM LAT. GLENOSPHERE 42XØ27
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code HSD·October 14, 2021