10 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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KENDALL FAST-CATH PRE LUBRICATED URETHRAL CATHETER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ZAVATION
FDA UDI
Zavation LLC·00842166117846·3.5mm x 46mm Polyaxial Shaft Screw
VES-TEMP MODEL VT1 MONOPLACE COOL/HEAT SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
IMPALA CASTERS
FDA 510(k)
FDA Class 1
·Physical Medicine
CAPIOX HEMOCONCENTRATOR
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code KDI·March 3, 2016
SEE H10
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code NBC·April 18, 2013
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE·Product code KDJ·February 22, 2013
7900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·January 19, 2011
FOLFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·August 1, 2014
1.85MM TI MATRIX SCREW SELF-TAPPING/4MM
FDA Adverse Event
Malfunction
·SYNTHES (USA)·Product code JEY·January 21, 2015