9 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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A.M.T. G-TUBE BALLOON REPLACEMENT GASTROSTOMY FEEDING DEVICE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Brigade
FDA UDI
Nuvasive, Inc.·00887517402523·Brigade Implant, 14x34x28mm 12°
PEEK Corpectomy
FDA UDI
Nuvasive, Inc.·00887517623898·PEEK Corp Core, Ø14x34mm
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704293401·
ROCCIA® MultiLIF
FDA 510(k)
FDA Class 2
·Orthopedic
MULTI-CAVITY EQUILIBRIUM CELL
FDA 510(k)ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·ANIMAS CORP.·Product code LZG·January 13, 2011
ABBOTT CLINICAL CHEMISTRY ICT CALIBRATOR
FDA Adverse Event
Malfunction
·ABBOTT MANUFACTURING INC·Product code JGS·July 31, 2014
FLUOROSCOPIC X-RAY
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·October 5, 2007