7 results
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19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Catapult Guide Sheath
FDA 510(k)
FDA Class 2
·Cardiovascular
MICROPLEX COIL SYSTEMS (MCS)
FDA 510(k)
FDA Class 2
·Neurology
MASIMO SET USPO2 PULSE OXIMETRY CABLE
FDA 510(k)
FDA Class 2
·Cardiovascular
CONTOUR TEST STRIPS (50)
FDA Adverse Event
Injury
·BAYER HEALTHCARE LLC·Product code NBW·November 4, 2008
EPIC II CRITICAL CARE BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·July 21, 2011
PAINSMART IOD
FDA Adverse Event
Malfunction
·MOOG DEVICE GROUP·Product code FRN·July 5, 2013
Model Number L111, ESSENTIO DR SL MRI Pacemaker
FDA Enforcement
Class I
·Ongoing·Boston Scientific Corporation·October 22, 2025