27 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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EMS SWISS LITHOCLAST MASTER (A.K.A. SWISS LITHOCLAST ULTRA)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
CERASMART™
FDA UDI
Gc America Inc.·14548161320283·CERASMART™ 270 14 Cerec A2 HT 5p Block
CERASMART®
FDA UDI
Gc America Inc.·D0470124451·CERASMART 270 14 CEREC A2 HT 5p
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151644·NC TREK Coronary Dilatation Catheter 2.0 mm x 1...
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151637·NC TREK Coronary Dilatation Catheter 2.0 mm x 8...
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151668·NC TREK Coronary Dilatation Catheter 2.0 mm x 2...
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151620·NC TREK Coronary Dilatation Catheter 2.0 mm x 6...
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151651·NC TREK Coronary Dilatation Catheter 2.0 mm x 1...
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033399088·
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033399101·
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033399095·
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033399071·
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361011699·PedFuse Respond, CNL, 8.0mm x 45mm
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033399064·
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033399118·
LIFEPAK 12DEFIBERLLATOR/MONITOR SERIES
FDA 510(k)
FDA Class 3
·Cardiovascular
PRECISE NITINOL STENT TRANSHEPATIC BILLARY SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
DEPTH DEVICE, 2.7 / 3.5 / 4.0MM, LOW PRO
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HTJ·July 11, 2025
E SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·February 19, 2013
SPRINT FIDELIS
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·March 9, 2011