7 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TRIMED 510 APNEA MONITOR
FDA 510(k)
FDA Class 2
·Anesthesiology
Aquilion Serve (TSX-307A/1) V1.2 with AiCE-i
FDA 510(k)
FDA Class 2
·Radiology
NELLCOR N-200 PULSE OXIMETER, MODEL N-200
FDA 510(k)
FDA Class 2
·Cardiovascular
ARCHITECT I2000 ANALYZER
FDA Adverse Event
Other
·ABBOTT LABORATORIES·Product code JJE·August 12, 2003
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR PURITAN·Product code CBK·February 5, 2014
PRECISION®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·November 7, 2012
DUR MAR +4 NEUT LNR 36X54
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LPH·August 25, 2010