8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BBL MGIT PRODUCTS
FDA 510(k)
FDA Class 1
·Microbiology
BD BBL¿ MGIT¿ OADC ENRICHMENT
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code MDB·May 13, 2024
SUTURE REMOVAL KIT
FDA 510(k)
FDA Class 2
·General Hospital
ECUMOL ULTRAVIOLET FACE TANNING UNITS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
LYNX SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·February 11, 2013
DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·January 10, 2011
EON MINI
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·July 16, 2014
PROTEGE RX CAROTID STENT SYSTEM
FDA Adverse Event
Malfunction
·COVIDIEN·Product code NIM·October 1, 2020