7 results
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19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ORMCO SYSTEM 1+ (TM)
FDA 510(k)
FDA Class 2
·Dental
VARIAX
FDA UDI
Stryker GmbH·07613327614909·Volar Distal Radius Plate Insert, Left
WRIGHT POCKET DOPPLERS VASCULAR & OBSTETRIC
FDA 510(k)
FDA Class 2
·Cardiovascular
INTELLIVUE PATIENT MONITOR MX400, INTELLIVUE PATIENT MONITOR MX450, INTELLIVUE PATIENT MONITOR MX500, INTELLIVUE PATIENT
FDA 510(k)
FDA Class 2
·Cardiovascular
SAPPHIRE
FDA Adverse Event
Malfunction
·SPINAL ELEMENTS, INC.·Product code KWQ·June 18, 2014
LIFEPAK 12 DEFIBRILLATOR/MONITOR SERIES
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code MKJ·December 8, 2010
CAUTERY UNIT
FDA Adverse Event
Injury
·PENTAX MEDICAL CO.·Product code HAM·October 17, 2006