6 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MODIFIED OSCOR PY PACING LEADS
FDA 510(k)
FDA Class 3
·Cardiovascular
Flex Robotic System and Flex Colorectal Drive
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
HI-TEMP LOOPTIP SURGICAL CAUTERY
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·December 10, 2012
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORP·Product code FRN·January 23, 2014
RENAL - DISPOSABLE
FDA Adverse Event
Injury
·Product code KDJ·October 8, 2010