10,000 results
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64ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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USA Elite
FDA UDI
Gyrus ACMI, LLC·00821925003521·USA Elite System and USA Series Ellik Evacuator...
USA Elite
FDA UDI
Gyrus ACMI, LLC·00821925003545·USA Elite System and USA Series Ellik Evacuator...
NEUROSEARCH-24 OR NRS-24
FDA 510(k)
FDA Class 2
·Neurology
NEUROSEARCH-24 OR NRS-24
FDA 510(k)
FDA Class 2
·Neurology
SCHELL C.A.P.P. BED MODEL NRS. 1268 + 1269
FDA 510(k)
FDA Class 2
·Physical Medicine
GORE HYBRID VASCULAR GRAFT
FDA Adverse Event
Malfunction
·W.L. GORE & ASSOCIATES·Product code DSY·November 1, 2012
GORE HYBRID VASCULAR GRAFT
FDA Adverse Event
Malfunction
·W.L. GORE & ASSOCIATES·Product code DSY·September 14, 2011
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·May 17, 2013
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·May 17, 2013
GORE HYBRID VASCULAR GRAFT
FDA Adverse Event
Malfunction
·W.L. GORE & ASSOCIATES·Product code DSY·December 5, 2012
GORE® HYBRID VASCULAR GRAFT
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code DSY·July 1, 2016
STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LGW·January 6, 2017
GORE® HYBRID VASCULAR GRAFT
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code DSY·November 12, 2014
GORE HYBRID VASCULAR GRAFT
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code DSY·August 29, 2011
GORE HYBRID VASCULAR GRAFT
FDA Adverse Event
Malfunction
·W.L. GORE & ASSOCIATES·Product code DSY·July 11, 2011
INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·May 23, 2014
GORE HYBRID VASCULAR GRAFT
FDA Adverse Event
Malfunction
·W.L. GORE & ASSOCIATES·Product code DSY·March 13, 2013
GORE HYBRID VASCULAR GRAFT
FDA Adverse Event
Malfunction
·W.L. GORE & ASSOCIATES·Product code DSY·June 20, 2013
GORE HYBRID VASCULAR GRAFT
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code DSY·December 2, 2011
GORE® HYBRID VASCULAR GRAFT
FDA Adverse Event
Malfunction
·W.L. GORE & ASSOCIATES·Product code DSY·December 28, 2016