28 results
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42ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TRIDENT ALL POLY CUP
FDA 510(k)
FDA Class 2
·Orthopedic
LIFEPAK® 15 monitor/defibrillator
FDA UDI
PHYSIO-CONTROL, INC.·00883873871706·15AABBABBABBBBAAAAAAAAAFLP15 MONITOR/DEFIB
OLYMPIC WARM-UP
FDA 510(k)
FDA Class 2
·Physical Medicine
MODIFICATION TO SCIMED 6F IMPULSE ANGIOGRAPHIC CATHATERS
FDA 510(k)
FDA Class 2
·Cardiovascular
9616240-2006-00341
FDA Adverse Event
Malfunction
·Product code FII·June 14, 2006
9616240-2006-00332
FDA Adverse Event
Other
·Product code FII·June 1, 2006
PHOENIX
FDA Adverse Event
Malfunction
·GAMBRO DASCO·Product code FII·May 10, 2006
9616240-2006-00339
FDA Adverse Event
Malfunction
·Product code FII·June 9, 2006
9616240-2006-00340
FDA Adverse Event
Malfunction
·Product code FII·June 9, 2006
9616240-2006-00350
FDA Adverse Event
Malfunction
·Product code FII·June 23, 2006
9616240-2006-00345
FDA Adverse Event
Malfunction
·Product code FII·June 14, 2006
VENTAK MINI+
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS·Product code LWS·August 5, 1998
ENDOTAK C
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS·Product code LWS·May 5, 1998
SUBCUTANEOUS PATCH
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS·Product code LWS·May 5, 1998
PHOENIX
FDA Adverse Event
Malfunction
·GAMBRO DASCO·Product code FII·May 10, 2006
PHOENIX
FDA Adverse Event
Malfunction
·GAMBRO DASCO·Product code FII·May 10, 2006
PUMP IN STYLE ADVANCED BREAST PUMP GO TOTE
FDA Adverse Event
Malfunction
·MEDELA, INC.·Product code HGX·March 11, 2013
PRECISION XTRA
FDA Adverse Event
Malfunction
·Product code NBW·February 27, 2011
EDGE INSUL COATED NEEDLE
FDA Adverse Event
Injury
·COVIDIEN LP (VALLEYLAB)·Product code GEI·February 20, 2008
TECNIS SIMPLICITY
FDA Adverse Event
Injury
·AMO PUERTO RICO MFG. INC.·Product code HQL·July 16, 2025