9 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ACUSON Juniper Diagnostic Ultrasound System and ACUSON Juniper Select Diagnostic Ultrasound System
FDA 510(k)
FDA Class 2
·Radiology
PT-S TEST STRIPS FOR THE COAGUCHEK SYSTEM, MODEL# 2032422
FDA 510(k)
FDA Class 2
·Hematology
CONTOUR NEXT BLOOD GLUCOSE METER
FDA 510(k)
FDA Class 2
·Clinical Chemistry
CONTOUR
FDA Adverse Event
Malfunction
·BAYER HEALTHCARE LLC·Product code NBW·April 29, 2014
CONTOUR
FDA Adverse Event
Malfunction
·ASCENSIA DIABETES CARE US INC.·Product code NBW·April 5, 2019
TAXUS (TM) LIBERTÉ (TM)
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·August 24, 2011
NC TREK CORONARY DILATATION CATHETER
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code LOX·November 3, 2014
M2A 38MM MOD HD +3MM NK
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·July 11, 2013
SMR CTA HUMERAL HEAD Ø54 MM
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code KWS·May 17, 2023