756 results
·
19ms
·
Sources: EU EUDAMED, US FDA
BURN RESUSCITATION DECISION SUPPORT SYSTEM (BRDSS)
FDA 510(k)
FDA Class 2
·Anesthesiology
LARGE CANNULATED SCREWS
FDA UDI
Smith & Nephew, Inc.·03596010064059·CANNULATED HIP PIN 55MM
UNKNOWN
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·August 14, 2015
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970379·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970423·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970393·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172974032·UniTip High Resolution Catheter 12F
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970416·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970409·
PRE-POWDERED LATEX EXAMINATION GLOVES WITH PROTEIN LABELING CLAIM (180 UG/OR LESS)
FDA 510(k)
FDA Class 1
·General Hospital
SUPERCROSS MICROCATHETER (130 CM), SUPERCROSS MICROCATHETER (150 CM) MODEL 5300, 5301
FDA 510(k)
FDA Class 2
·Cardiovascular
TENDRIL ST
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, CRMD·Product code NVN·January 13, 2014
NGAGE
FDA Adverse Event
Malfunction
·COOK MEDICAL·Product code FFL·April 30, 2013
XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code NIQ·June 13, 2011
UNKNOWN
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·January 5, 2017
UNKNOWN
FDA Adverse Event
Malfunction
·WILLIAM COOK EUROPE·Product code DTK·December 15, 2015
UNKNOWN
FDA Adverse Event
Malfunction
·WILLIAM COOK EUROPE·Product code DTK·November 19, 2015
UNKNOWN
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·June 17, 2016
UNKNOWN
FDA Adverse Event
Injury
·COOK INC·Product code DTK·June 13, 2016
UNKNOWN
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·November 17, 2016