8 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ACS HI-TORQUE WHOLEY SUPRA CORE GUIDE WIRE
FDA 510(k)
FDA Class 2
·Cardiovascular
DeltaForm HD
FDA UDI
Merz Dental GmbH·D7091980119·DeltaForm HD lower posteriors, XS, C3 -MADE IN ...
NEBULIZER, DISP, 2D0815
FDA 510(k)
FDA Class 2
·Anesthesiology
CLEARSCAN
FDA 510(k)
FDA Class 2
·Radiology
FRESENIUS 2008K
FDA Adverse Event
Injury
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·June 25, 2014
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·February 27, 2013
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 24, 2011
1.85MM TI MATRIX SCREW SELF-TAPPING/4MM
FDA Adverse Event
Malfunction
·SYNTHES (USA)·Product code JEY·January 21, 2015