8 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SYNTHES SPINE OCCIPITAL-CERVICAL PLATE/ROD AND HOOK SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
PE anti-human CD45
FDA UDI
BIOLEGEND, INC.·00810034702432·URL: https://www.biolegend.com/en-us/products/p...
PROPELLER HEAD
FDA UDI
Biomet Orthopedics, LLC·00880304417045·
Duo Lumbar Interbody Fusion Device
FDA 510(k)
FDA Class 2
·Orthopedic
AIR ASSISTED SPRAYER, MODELS: AIRSPRAYUS01 AND AIRSPRAYUS
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
AUTOPULSE NIMH BATTERY
FDA Adverse Event
Malfunction
·ZOLL CIRCULATION, INC.·Product code DRM·January 25, 2013
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·August 5, 2014
IN TOUCH ZU
FDA Adverse Event
Malfunction
·STRYKER CORP., MEDICAL DIV.·Product code FNL·January 13, 2011