7 results
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19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CONTINUOUS FLUSH DEVICE
FDA 510(k)
FDA Class 2
·Cardiovascular
P.0004 IMPLANTS
FDA 510(k)
FDA Class 2
·Dental
RENASYS-G Gauze Dressing Kits with Soft Port
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
REF H10
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code MMI·August 9, 2016
INTERPULSE HANDPIECE WITH HIGH FLOW TIP
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS PUERTO RICO·Product code FQH·January 24, 2013
CELL-DYN 1800 ANALYZER
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·January 17, 2011
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·July 28, 2014