9 results
·
27ms
·
Sources: EU EUDAMED, US FDA
TASSI MK3 (TURNAIR)
FDA 510(k)
FDA Class 2
·Physical Medicine
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756378987·RO UNIVERSAL ORTHO PACK
REVERSE SHOULDER SYSTEM HUMERAL REVERSE HC LINER Ø36/+3MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code PHX·December 13, 2021
HARRISON HAND HELD ADJUSTING INSTRUMENT
FDA 510(k)
FDA Unclassified
·Unknown
HYDRASHIFT 2/4 daratumumab
FDA 510(k)
FDA Class 2
·Immunology
INDIGO 1.0CM LASER FIBER
FDA Adverse Event
Death
·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code GEX·June 22, 2006
INTERSTIM II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code EZW·January 11, 2013
MIRA CR4000 OPHTHALMIC CRYO UNIT
FDA Adverse Event
Malfunction
·MIRA, INC.·Product code GEH·November 23, 2010
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·July 2, 2014