9 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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S-ROM 135 FEMORAL STEM & COLLAR(PART OF S-ROM HIP
FDA 510(k)
FDA Class 2
·Orthopedic
SROM*STM ST,36+8L NK,22X17X165
FDA Adverse Event
Injury
·DEPUY IRELAND·Product code JDI·April 2, 2012
NAR Kit
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209103669·KIT, VISOR MED IPOK - REFILL ONLY
Sklar®
FDA UDI
SKLAR CORPORATION·10649111035272·OTIS DITTEL SOUND CVD 22FR
DUAL MODE UP-GRADE FOREHEAD/UNDERARM THERMOMETER DEVICE
FDA 510(k)
FDA Class 2
·General Hospital
Reform Pedicle Screw System
FDA 510(k)
FDA Class 2
·Orthopedic
EON
FDA Adverse Event
Injury
·ST. JUDE MEDICAL ¿ NEUROMODULATION·Product code GZB·May 22, 2014
HEARTSTART MRX-EMS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·October 30, 2012
STARCLOSE SE VASCULAR CLOSURE SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR - REDWOOD CITY·Product code MGB·September 29, 2010