12 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Bleep DreamPort
FDA 510(k)
FDA Class 2
·Anesthesiology
BANTAM CATHETER (280MM BALLOON LENGTHS)
FDA 510(k)
FDA Class 2
·Cardiovascular
ULTRASOUND SCANNER FLEX FOCUS 1202
FDA 510(k)
FDA Class 2
·Radiology
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·November 26, 2020
AVAULTA ANTERIOR BIOSYNTHETIC SUPPORT SYSTEM
FDA Adverse Event
Injury
·SOFRADIM PRODUCTIONS·Product code FTL·April 18, 2013
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 22, 2011
ANALYTICAL P MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·September 19, 2008
ADVANCE
FDA Adverse Event
Injury
·MEDTRONIC, INC·Product code DXE·September 9, 2019
MENTOR CPX4 WITH SUTURE TABS, TALL HEIGHT, SMOOTH
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code LCJ·October 24, 2019
MENTOR CPX4 WITH SUTURE TABS, MED HEIGHT, SMOOTH
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code LCJ·January 10, 2020
CPX4 PLUS SMOOTH TALL HEIGHT 550CC
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code LCJ·April 19, 2022
CPX4 WITH SUTURE TABS MEDIUM HEIGHT SMOOTH EXPANDER
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code LCJ·February 22, 2021