9 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PS MEDICAL CRANIAL HAND DRILL
FDA 510(k)
FDA Class 2
·Neurology
THE NAUTILUS NASAL IMPLANT
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MRT 50A SOFTWARE RELEASE 9.0
FDA 510(k)
FDA Class 2
·Radiology
COAGUCHEK ® XS SYSTEM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code GJS·January 9, 2013
QUATTRODE PERCUTANEOUS LEAD
FDA Adverse Event
Malfunction
·ADVANCED NEUROMODULATION SYSTEMS·Product code LGW·October 28, 2010
VITROS IMMUNODIAGNOSTIC PRODUCT TROPI ES REAGENT PACK
FDA Adverse Event
Malfunction
·ORTHO-CLINICAL DIAGNOSTICS·Product code MMI·July 1, 2014
TO GORE-TEX® STRETCH VASCULAR GRAFT
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code DSY·July 27, 2021
GORE-TEX® STRETCH VASCULAR GRAFT
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code DSY·July 27, 2021
GORE-TEX® STRETCH VASCULAR GRAFT
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code DSY·July 27, 2021