31 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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FIBREX CATHETER PATENCY DEVICE
FDA 510(k)
FDA Class 2
·General Hospital
NA
FDA UDI
GE Healthcare Finland Oy·00840682104456·
NA
FDA UDI
GE Healthcare Finland Oy·00840682104432·
NA
FDA UDI
GE Healthcare Finland Oy·00840682104463·
NA
FDA UDI
GE Healthcare Finland Oy·00840682104425·
Myo/Wire II
FDA UDI
A & E MEDICAL CORPORATION·10841291104834·SS Suture, 4 per sleeve
LORENZ FIDUCAIL SCREW
FDA 510(k)
FDA Class 2
·Neurology
AB BELT
FDA 510(k)
FDA Class 2
·Physical Medicine
ASR ACETABULAR CUPS 58
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·April 11, 2012
ASR ACETABULAR CUPS 48
FDA Adverse Event
Injury
·DEPUY INTL, LTD.·Product code KWA·December 29, 2010
ONIPOD INSULIN PUMP
FDA Adverse Event
Malfunction
·INSULET CORP·Product code LZG·March 12, 2013
840 VENTILATOR
FDA Adverse Event
Malfunction
·PURITAN-BENNETT IRELAND·Product code CBK·May 7, 2008
PRECISION XTRA
FDA Adverse Event
Malfunction
·Product code NBW·April 5, 2011
ASR UNI FEMORAL IMPL SIZE 51
FDA Adverse Event
Injury
·DEPUY INTL., LTD. - 8010379·Product code KWA·August 21, 2013
ASR ACETABULAR CUPS 60
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·October 24, 2015
ASR ACETABULAR CUPS 58
FDA Adverse Event
Injury
·DEPUY INTL., LTD. - 8010379·Product code KWA·August 21, 2013
ASR UNI FEMORAL IMPL SIZE 49
FDA Adverse Event
Injury
·DEPUY INTL., LTD. - 8010379·Product code KWA·July 22, 2013
ADAPTER SLEEVES 12/14 +8
FDA Adverse Event
Injury
·DEPUY INTL.,LTD 8010379·Product code KWA·November 4, 2015
ADAPTER SLEEVES
FDA Adverse Event
Injury
·DEPUY INTL.,LTD 8010379·Product code KWA·February 2, 2016
ASR ACETABULAR CUPS 56
FDA Adverse Event
Injury
·DEPUY INTL.,LTD 8010379·Product code KWA·February 2, 2016