9 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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FOUNDATION UNIPOLAR FEMORAL HEAD WITH MODULAR NECK LENGTH SLEEVES
FDA 510(k)
FDA Class 2
·Orthopedic
Penumbra Coil 400, Ruby Coil System, POD System
FDA 510(k)
FDA Class 2
·Neurology
WG-SURGICAL SUTURES WITH NEEDLE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
EON MINI
FDA Adverse Event
Injury
·ST JUDE MEDICAL - NEUROMODULATION·Product code LGW·February 19, 2013
6800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 19, 2011
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE·Product code KDJ·August 1, 2014
COULTER ACT PAK REAGENT KIT
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GKZ·September 24, 2014
COULTER ACT PAK REAGENT KIT
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GKZ·May 26, 2015
COULTER ACT PAK REAGENT KIT
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GKZ·May 5, 2015