7 results
·
18ms
·
Sources: EU EUDAMED, US FDA
EARCHECK
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704294248·
NEEDLE HOLDER, MICROVASCULAR
FDA 510(k)
FDA Class 1
·Gastroenterology, Urology
STRYKER CROSSFIRE SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
EON MINI
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·February 19, 2013
ACCU-CHEK ® AVIVA TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·January 27, 2011
TOTAL ASR ACET IMP SIZE 56
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·July 31, 2014