7 results
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19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Surefire Spark Infusion System
FDA 510(k)
FDA Class 2
·Cardiovascular
COMFORTRONIC 4894 AND COMFORTDRIVE 200XDA HANDPIECE
FDA 510(k)
FDA Class 1
·Dental
LYMPHA PRESS 201MAX, MODEL 201MAX
FDA 510(k)
FDA Class 2
·Cardiovascular
INVICTUS SPINAL FIXATION SYSTEM
FDA Adverse Event
Injury
·ALPHATEC SPINE, INC.·Product code NKB·April 30, 2025
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 15, 2014
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·June 20, 2013
VASOVIEW HEMOPRO EVH SYSTEM
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR, LLC·Product code GEI·July 7, 2011