7 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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IUC - INTRAUTERINE CATHETER
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
SUNPOLAR HEALTHLINE, MODEL 100; COMPFRESH, MODEL 200; NATUREX , MODEL 300; AND IHEALTH, MODEL 400 STOCKINGS
FDA 510(k)
FDA Class 2
·General Hospital
MEP Monitor
FDA 510(k)
FDA Class 2
·Neurology
BD DISC CEFTAZIDIME CAZ-30 JAPAN
FDA Adverse Event
Malfunction
·BECTON DICKINSON CARIBE LTD.·Product code JTN·January 18, 2022
ENTRUST AT
FDA Adverse Event
MEDTRONIC MED REL, INC.·Product code LWS·October 9, 2010
ARDIS INSERTER - 9MM
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code MAX·February 19, 2014
MEGA SUTURECUT NEEDLE DRIVER INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·December 10, 2012