9 results
·
18ms
·
Sources: EU EUDAMED, US FDA
RIA, T3 UPTAKE SOLID PHASE
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Iridex TruFocus LIO Premiere
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
AUTOMATIC ANALYZER
FDA 510(k)
FDA Class 1
·Clinical Chemistry
ZILVER PTX DRUG-ELUTING PERIPHERAL STENT
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code NIU·November 3, 2017
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 30, 2014
UNKNOWN DEPUY ASR FEMORAL HEAD
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KXA·October 10, 2012
TOTAL ASR FEM IMP SIZE 51
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD - 8010379·Product code KXA·May 19, 2015
ZILVER PTX DRUG-ELUTING PERIPHERAL STENT
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code NIU·December 24, 2015
ZILVER PTX DRUG-ELUTING PERIPHERAL STENT
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code NIU·December 30, 2015