7 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BIO-PLEXUS DROP-IT NEEDLE HOLDER
FDA 510(k)
FDA Class 2
·General Hospital
THERMOMED 1.8
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
HOSPITAL BED
FDA 510(k)
FDA Class 1
·General Hospital
2008K2 HEMODIALYSIS SYS. OLC/DIASAFE PLS
FDA Adverse Event
Malfunction
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·May 7, 2014
ENVOY DISTAL ACCESS GUIDING CATHETER
FDA Adverse Event
Malfunction
·CODMAN AND SHURTLEFF, INC·Product code DQY·February 15, 2013
VALVE AORTIC MAGNA TFX 25MM
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·January 12, 2011
2.5 mm Reaming Rod W/Ball Tip 650 mm, Sterile
FDA Enforcement
Class II
·Terminated·Synthes (USA) Products LLC·November 30, 2016