8 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VANISHPOINT SYRINGE
FDA 510(k)
FDA Class 2
·General Hospital
DeltaForm HD
FDA UDI
Merz Dental GmbH·D7091980069·DeltaForm HD lower posteriors, XS, B2 -MADE IN ...
HDR MRI Lumen Marker
FDA 510(k)
FDA Class 2
·Radiology
DIMERTEST
FDA 510(k)
FDA Class 2
·Hematology
DASHER -14 STEERABLE GUIDEWIRE
FDA Adverse Event
Injury
·NEUROVASCULAR, A DIVISION OF BOSTON SCIENTIFIC CORP·Product code DQX·January 9, 2007
OCTRODE
FDA Adverse Event
Injury
·ST JUDE MEDICAL - NEUROMODULATION·Product code LGW·February 22, 2013
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 2, 2014
9600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 24, 2011