7 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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3DIEMME RealGUIDE
FDA 510(k)
FDA Class 2
·Radiology
Sklar®
FDA UDI
SKLAR CORPORATION·10649111017872·CAIRNS HEMO&SCALP FCP CVD 6"
RELIEVA AND RELIEVA ACELLA SINUS BALLOON CATHETER
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
VACUETTE BLOOD COLLECTION TUBE WITH LITHIUM HEPARIN AND GEL SEPARATOR
FDA 510(k)
FDA Class 2
·Clinical Chemistry
RESOLUTION CLIP CLIPPING DEVICE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code MND·July 23, 2011
GYNECARE PROLIFT PELVIC FLOOR REPAIR SYSTEM
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTP·June 17, 2013
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 19, 2008