7 results
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18ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
INERPAN(TM) TEMPORARY WOUND DRESSING
FDA 510(k)
FDA Unclassified
·Unknown
PERFSCAPE V2.0
FDA 510(k)
FDA Class 2
·Radiology
MODIFICATION TO THE EMIT II PLUS PHENCYCLIDINE ASSAY, MODEL OSR9J229
FDA 510(k)
FDA Unclassified
·Unknown
SYRINGE 10ML LS EMERALD
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·February 8, 2021
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 13, 2015
RENAL - DISPOSABLE
FDA Adverse Event
Injury
·Product code KDJ·November 30, 2010
R SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·December 7, 2012