10 results
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54ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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SetPoint Medical Corporation
FDA registration
SetPoint Medical Corporation·1 product·🇺🇸 United States
SetPoint Programmer
FDA UDI
SetPoint Medical Corporation·00860013950248·
SetPoint Charger
FDA UDI
SetPoint Medical Corporation·00860013950224·
SetPoint Charger and Docking Station
FDA UDI
SetPoint Medical Corporation·00860013950217·
SetPoint Implant
FDA UDI
SetPoint Medical Corporation·00860013950200·
SetPoint Docking Station
FDA UDI
SetPoint Medical Corporation·00860013950231·
AUTOPULSE RESUSCITATION SYSTEM MODEL 100
FDA Adverse Event
Malfunction
·ZOLL CIRCULATION, INC.·Product code DRM·September 28, 2012
ATLAS CONTROLLER
FDA Adverse Event
Injury
·ARTHROCARE CORP.·Product code GEI·August 28, 2007
ATLAS CONTROLLER
FDA Adverse Event
Other
·ARTHROCARE CORP.·Product code GEI·May 24, 2007
Glucose Oxidase Reagent as follows: Pointe Scientific Glucose Oxidase Reagent Set, Pointe Scientific, Inc, Canton, MI; Catalog # G7519-1L, G7519-500 and G7519-SAM. 2MM Diagnostics Glucose Oxidase Reagent Set, 2MM Corporation, Miami, FL; Reorder # RT-160-500. Pointe Scientific Glucose Oxidase Reagent, Pointe Scientific, Inc., Canton, MI; Catalog, MI; Catalog # 2-G7519-L, 7-G7519-100, 7-G7519-200, 7-G7519-1000, 8-G7519-100, and 12-RT-160-500. For the quantitative determination of Glucose in human serum. For in vitro diagnostic use only.
FDA Recall
Terminated
·Pointe Scientific, Inc.·Product code CGA·November 3, 2008