7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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THE SAFETY 1ST DIGITAL PACIFIER
FDA 510(k)
FDA Class 2
·General Hospital
Fully Automatic Electronic Blood Pressure Monitor
FDA 510(k)
FDA Class 2
·Cardiovascular
CLINITEK ADVANTUS, MODEL 1420
FDA 510(k)
FDA Class 2
·Clinical Chemistry
BONE ANCHOR SYSTEM FOR SOFT TISSUE SUPPORT
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - SPENCER·Product code MBI·April 27, 2012
SSP UNITRAY KIT HR HLA-DQB1 WITH TAQ
FDA Adverse Event
Malfunction
·LIFE TECHNOLOGIES CORPORATION·Product code MZI·June 18, 2014
CONSERVE(R) PLUS CUP
FDA Adverse Event
Injury
·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KWA·February 15, 2013
PULSE GEN MODEL 102
FDA Adverse Event
Injury
·CYBERONICS, INC.·Product code LYJ·January 13, 2011