25 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ENTRY SITE ALIGNMENT SYSTEM MODEL # CX9626
FDA 510(k)
FDA Class 1
·Ophthalmic
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151149·NC TREK Coronary Dilatation Catheter 2.50 mm x ...
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151132·NC TREK Coronary Dilatation Catheter 2.50 mm x ...
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151187·NC TREK Coronary Dilatation Catheter 2.50 mm x ...
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151163·NC TREK Coronary Dilatation Catheter 2.50 mm x ...
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151156·NC TREK Coronary Dilatation Catheter 2.50 mm x ...
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151170·NC TREK Coronary Dilatation Catheter 2.50 mm x ...
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033408872·
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033408889·
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033408841·
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361011675·PedFuse Respond, CNL, 8.0mm x 35mm
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033408858·
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033408865·
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033408896·
MODIFICATION TO AXYA MEDICAL, INC. BONE ANCHOR SYSTEM AND KIT (BAK)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PHILIPS BV PULSERA/ENDURA
FDA 510(k)
FDA Class 2
·Radiology
TREK CORONARY DILATATION CATHETER
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR·Product code LOX·October 1, 2021
IPC® STYLUS TRANSNASAL BUR
FDA Adverse Event
Death
·MEDTRONIC XOMED INC.·Product code ERL·February 4, 2015
SYNCARDIA TEMPORARY TOTAL ARTIFICIAL HEART
FDA Adverse Event
Other
·SYNCARDIA SYSTEMS, INC.·Product code LOZ·September 25, 2012
AXXESS
FDA Adverse Event
Injury
·ST JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 15, 2013