6 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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APPLICATOR, LEE IMPRESSION
FDA 510(k)
FDA Class 1
·Dental
WiScope Digital Endoscope System
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PROSIT WOUND TREATMENT DEVICE
FDA 510(k)
FDA Unclassified
·Unknown
XIENCE PRIME EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code NIQ·April 30, 2014
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC, USA·Product code LFR·June 26, 2007
ACCU-CHEK SPIRIT COMBO
FDA Adverse Event
Malfunction
·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·October 5, 2012