8 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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H-H ATRIAL CATHETERS & PERITONEAL CATHETERS
FDA 510(k)
FDA Class 2
·Neurology
Stainless Steel Wire
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746047312·WIRE SS UPPER 016 X 016 FORM II 10/PK
NAR
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209118892·
AMS MALE TRANSOBTURATOR SLING SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Sonicision Cordless Ultrasonic Dissection Device
FDA 510(k)
FDA Unclassified
·Unknown
MED-EL COMBI 40+ COCHLEAR IMPLANT SYMSTEM
FDA Adverse Event
Malfunction
·MED-EL ELEKTROMEDIZINISCHE GERAETE, GMBH·Product code MCM·April 7, 2014
PUMP MMT-722NAL PRDGM INS V2.2 CL EN PR
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·October 1, 2010
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE·Product code KDJ·November 30, 2012