63 results
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34ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PCA-C1 series Patient Cable
FDA 510(k)
FDA Class 2
·Cardiovascular
RMO
FDA UDI
Rmo, Inc.·00885797100122·REMOV QUADHELIX KIT
OsteoMed
FDA UDI
OSTEOMED LLC·00845694017848·MFx 2.4 Fracture Organizer Block
UNIPOLAR NEEDLES
FDA 510(k)
FDA Class 2
·Anesthesiology
TELAVANCIN 30 UG, BBL SENSI-DISC
FDA 510(k)
FDA Class 2
·Microbiology
DEEP BRAIN STIMULATION LEAD
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·February 5, 2008
DEEP BRAIN STIMULATION LEAD
FDA Adverse Event
Death
·MEDTRONIC NEUROMODULATION·Product code MHY·December 5, 2007
DEEP BRAIN STIMULATION LEAD
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·March 27, 2008
DEEP BRAIN STIMULATION LEAD
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·December 5, 2007
ITREL II
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·March 6, 2008
DEEP BRAIN STIMULATION LEAD
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·February 5, 2008
ITREL II
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·March 6, 2008
DEEP BRAIN STIMULATION LEAD
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·March 19, 2008
DEEP BRAIN STIMULATION LEAD
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·March 19, 2008
DEEP BRAIN STIMULATION LEAD
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·March 19, 2008
DEEP BRAIN STIMULATION LEAD
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·March 19, 2008
DEEP BRAIN STIMULATION LEAD
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·March 19, 2008
DEEP BRAIN STIMULATION LEAD
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·March 19, 2008
DEEP BRAIN STIMULATION LEAD
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·March 19, 2008
DEEP BRAIN STIMULATION LEAD
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·March 19, 2008