8 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ENDIUS SPINE ENDOSCOPE
FDA 510(k)
FDA Class 2
·Neurology
DERMATOLOGIC TREATMENT SYSTEM (DTS) G2
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Decanting Device
FDA 510(k)
FDA Class 2
·General Hospital
CADD-LEGACY® PCA AMBULATORY INFUSION PUMP
FDA Adverse Event
Injury
·SMITHS MEDICAL ASD INC.,·Product code MEA·March 29, 2016
ASCENT SYSTEM-BEARING
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·December 28, 2016
SECURE II MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·January 4, 2013
ACCU-CHEK ® AVIVA TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·February 9, 2011
ARTERIAL LINE KIT
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL INC.·Product code DQX·July 2, 2014