7 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Transcutaneous Electrical Nerve Stimulator, Model: KTR-405
FDA 510(k)
FDA Class 2
·Neurology
SOLSTICE CROSS CONNECTOR
FDA 510(k)
FDA Class 2
·Orthopedic
SARNS CENTRIFUGAL PUMP WITH XCOATING, MODEL 164275X
FDA 510(k)
FDA Class 2
·Cardiovascular
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 30, 2024
MULTI-LINK RX VISION CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MAF·August 23, 2011
ELLIPSE VR, DF-4 CONNECTOR
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·November 3, 2014
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Death
·BAXTER HEALTHCARE·Product code KDJ·July 11, 2013