8 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Crossing Support Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
CoRoent
FDA UDI
Nuvasive, Inc.·00887517639035·CoRoent Ant TLIF PEEK, 8x13x30mm 15°
ONE TOUCH PROFILE
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·January 6, 2003
PENUMBRA EMBOLIZATION COIL SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
POWDER FREE NITRILE EXAMINATION GLOVES, STERILE WITH CHEMOTHERAPY CLAIM
FDA 510(k)
FDA Class 1
·General Hospital
ANSPACH XMAX
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code ERL·October 17, 2014
TI DHS®/DCS® LAG SCREW 12.7MM THREAD/90MM
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code JDO·June 21, 2013
PRECISION XTRA
FDA Adverse Event
Malfunction
·Product code NBW·July 28, 2011