6 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ELECTRO-MYOGRAPHIC PERINEOMETER
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
JAKOBI SURG. INSTRUMENTS #2 70/71
FDA 510(k)
FDA Class 2
·General Hospital
QUINTON INJECTION SEALING CAP
FDA 510(k)
FDA Class 2
·General Hospital
EASYPUMP II
FDA Adverse Event
Malfunction
·B. BRAUN MELSUNGEN AG·Product code MEB·May 29, 2014
PULSE GEN MODEL 103
FDA Adverse Event
Injury
·CYBERONICS, INC.·Product code LYJ·December 3, 2012
TERUMO CDI 500 BLOOD PARAMETER MONITOR
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·September 3, 2010