9 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ESOFLIP BALLOON DILATION CATHETER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Oticon
FDA UDI
Oticon A/S·05707131258861·H15, MINIRITE 312 WL CNB
SYNTHETIC VINYL EXAMINATION GLOVES, POWDER FREE
FDA 510(k)
FDA Class 1
·General Hospital
HEMEDEX CRANIAL BOLT MODELS, 3601, 3602
FDA 510(k)
FDA Class 2
·Neurology
INGENIO
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·October 1, 2014
PROLIFT PELVIC FLOOR REPAIR
FDA Adverse Event
Injury
·ETHICON, INC.·Product code OTP·May 29, 2013
RENAISSANCE 26 STRETCHER
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FPO·June 13, 2011
PINNACLE MTL INS NEUT36IDX54OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·January 27, 2012
ARTICULEZE M HEAD 36MM +5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·January 27, 2012