6 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Stimulation System (PA series, PR series, S series and Q series)
FDA 510(k)
FDA Class 2
·Physical Medicine
LevaLap Laparoscopic Access Device
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Dental Low-speed Handpieces and Accessories
FDA 510(k)
FDA Class 1
·Dental
FENESTRATED BIPOLAR FORCEPS INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL, INC.·Product code GEI·November 14, 2008
POWER PRO AMBULANCE COT
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code INK·July 19, 2011
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 18, 2013