6 results
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21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PRO CHECK DIGITAL PACIFIER THERMOMETER
FDA 510(k)
FDA Class 2
·General Hospital
PulsioFlex Monitoring System
FDA 510(k)
FDA Class 2
·Cardiovascular
OPHTHALMOSCOPE F-10
FDA 510(k)
FDA Class 2
·Ophthalmic
GLUCOCARD VITAL BLOOD GLUCOSE SYSTEM
FDA Adverse Event
Injury
·ARKRAY, INC.·Product code NBW·February 21, 2013
GORE EXCLUDER AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·January 20, 2011
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 31, 2014