7 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BABYPAC
FDA 510(k)
FDA Class 2
·Anesthesiology
artegral
FDA UDI
Merz Dental GmbH·D7091970158·anteriors; shade B1; mould IL
PowerGlide ST Midline Catheter
FDA 510(k)
FDA Class 2
·General Hospital
R-PORT LAPAROSCOPIC ACCESS DEVICE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
HEARTSTART XL+DEFIBRILLATOR/MONITOR
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 29, 2014
PINNACLE PELVIC FLOOR REPAIR KITS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·February 20, 2013
SYNCHROMED EL
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·January 14, 2011