7 results
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19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Digital Thermometer
FDA 510(k)
FDA Class 2
·General Hospital
ULTRAEKOGEL MODELS EK 2000 & EK 2001
FDA 510(k)
FDA Class 2
·Radiology
SPLIT CATH RG
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MINICAP PD TRANSFER SET (EASY-LOCK) WITH TWIST CLAMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code KDJ·November 17, 2008
XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Death
·AV-TEMECULA-CT·Product code NIQ·September 1, 2011
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 17, 2013
DUR OPT LPW POLY INS 28/54,56
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·February 5, 2019