7 results
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28ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
MEDFLATOR II(TM) DISPOSABLE INFLATION DEVICE
FDA 510(k)
FDA Class 2
·Cardiovascular
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471122963·K-WIRE - SINGLE TROCAR 0.9mm DIA x 150mm
MODIFICATION TO ENCOMPASS
FDA 510(k)
FDA Class 2
·Radiology
VAPR ARCTIC SUCTION ELECTRODE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
6800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 16, 2013
MARATHON MICRO CATHETER
FDA Adverse Event
Injury
·EV3 NEUROVASCULAR·Product code KRA·December 23, 2010
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEATHCARE CORPORATION·Product code FKX·July 17, 2014