7 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LINICAL PROTEIN III CALIBRATION VERIFIERS LEVELS A-E FOR BECKMAN ARRAY PROTEIN SYSTEM
FDA 510(k)
FDA Class 2
·Immunology
Diacore
FDA 510(k)
FDA Class 2
·Physical Medicine
NEOCARE MODEL 800 INFANT RADIANT WARMER
FDA 510(k)
FDA Class 2
·General Hospital
PREMIUM SURGICLIP S-9.0 TITANIUM
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY USSC PUERTO RICO·Product code FZP·February 6, 2013
ICL (IMPLANTABLE COLLAMER LENS)
FDA Adverse Event
Malfunction
·STAAR SURGICAL COMPANY·Product code MTA·July 23, 2014
VENTAK PRIZM
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 10, 2011
ev3 Pipeline Flex Embolization Device with Shield Technology. Sold OUS. For neurological endovascular use.
FDA Enforcement
Class I
·Terminated·Micro Therapeutics Inc, Dba Ev3 Neurovascular·April 1, 2020