7 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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!M1
FDA 510(k)
FDA Class 2
·Radiology
LEVA (TM) SPACER SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
MSI S-500L RF GENERATOR
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BD VACUTAINER® URINE ANALYSIS PRESERVATIVE TUBE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code KDT·February 12, 2020
FLOGARD
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·November 10, 2014
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE·Product code KDJ·September 9, 2011
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·July 23, 2013