8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NEUROLOGICAL ENDOSCOPE
FDA 510(k)
FDA Class 2
·Neurology
artegral
FDA UDI
Merz Dental GmbH·D7091970162·anteriors; shade B1; mould ITM
FORCETRIAD ELECTROSURGICAL GENERATOR; LIGASURE INSTRUMENTS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Vesco Medical Nasoenteric Feeding Tubes
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MENTOR MEMORYGEL BREAST IMPLANT
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FTR·January 8, 2020
HEARTSTART XL+ DEFIBRILLATOR/MONITOR
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 29, 2014
ACCU-CHEK ® MULTICLIX
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code FMK·February 20, 2013
AMISTEM H FEMORAL STEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·January 14, 2011