9 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
SET, ADMINISTRATION, INTRAVASCULAR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FPA·June 6, 2016
INTERLINK SYSTEM LEVER LOCK CANNULA WITH CHECK VALVE, SECONDARY MEDICATION SETS, SOLUTION SETS, CONTINU-FLO SOLUTION SET
FDA 510(k)
FDA Class 2
·General Hospital
DAN KERRISON RONGEURS, MODELS K1 + BILLY 1
FDA 510(k)
FDA Class 2
·Neurology
EPLUS SKIN TREATMENT SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PROSOUND F75 ULTRASOUND SCANNER
FDA Adverse Event
Malfunction
·HITACHI ALOKA MEDICAL, LTD·Product code GXX·July 16, 2014
TECH ATTACH CABLE
FDA Adverse Event
Malfunction
·AD TECH MEDICAL INSTRUMENT·Product code IKD·May 15, 2013
CAPSUREFIX NOVUS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 14, 2011
SYNERGY
FDA Adverse Event
Malfunction
·MEDTRONIC SWISS MANUFACTURING FACILITY·Product code LGW·August 15, 2008
MEGA 7.5FR. 40CC
FDA Adverse Event
Malfunction
·DATASCOPE CORP. - FAIRFIELD·Product code DSP·February 10, 2020