7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LM ANCHOR
FDA 510(k)
FDA Class 2
·Orthopedic
PAD, COOLING #27-999
FDA 510(k)
FDA Class 2
·Cardiovascular
FC-101 FEMORAL CATHETER GUIDE WIRE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.35 WIRE, 12, STERILE
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code GCP·August 11, 2021
MINI-CAP
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·February 27, 2013
ENDOPLEDGE CORONARY SINUS CATHETER
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES·Product code DWF·February 8, 2011
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·August 5, 2014