7 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AESKULISA DS DNA G
FDA 510(k)
FDA Class 2
·Immunology
SONOSITE HAND-CARIED UNTRASOUND SYSTEM (POWERSERIES)
FDA 510(k)
FDA Class 2
·Radiology
CONCORD 82
FDA 510(k)
FDA Class 2
·Dental
MAXIFLO ULTRATHIN WITH UNITY CONTRUCTION
FDA Adverse Event
Injury
·VASCUTEK LTD.·Product code DSY·August 27, 2012
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE·Product code KDJ·April 8, 2013
8800
FDA Adverse Event
Malfunction
·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD·Product code JAA·March 24, 2011
LARGE EPICARDIAL PATCH LEAD
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS, INC·Product code LWS·May 8, 2008