7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ENERGIZED DRUG CONTAINER SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471156050·K-WIRE - SINGLE TROCAR 1.1mm DIA x 230mm
UniSpace® Stand-Alone C Cage
FDA 510(k)
FDA Class 2
·Orthopedic
MCCOY CELLS
FDA 510(k)
FDA Class 1
·Hematology
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 3, 2013
ENDOVIVE TWO-PORT TTP JEJUNAL FEEDING TUBE CAP
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - SPENCER·Product code KNT·December 21, 2010
WIRELESS BATTERY MODULE G
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 1, 2014