1,167 results
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19ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ARROW EPIDURAL CATHETERIZATION KIT
FDA Adverse Event
Injury
·ARROW INTERNATIONAL LLC·Product code BSO·February 14, 2025
Culture Media, Antifungal, Susceptibility Test
FDA classification
FDA Class 2
·Culture Media, Antifungal, Susceptibility Test
MIE GMBH
FDA registration
MIE GMBH·2 products·🇩🇪 Germany
MJM INTERNATIONAL CORPORATION
FDA registration
MJM INTERNATIONAL CORPORATION·10 products·🇺🇸 United States
MIE AMERICA, INC.
FDA registration
MIE AMERICA, INC.·2 products·🇺🇸 United States
MDE ESCORT 1000 & MDE ESCOR 2000
FDA 510(k)
FDA Class 2
·Cardiovascular
CIM M4E
FDA UDI
Medical Measurement Systems B.V.·08717775955658·
ZACROS CORPORATION MIE FACILITY
FDA registration
ZACROS CORPORATION MIE FACILITY·1 product·🇯🇵 Japan
Ventlab
FDA UDI
VENTLAB, LLC·10889483555675·AirFlow Pediatric Resuscitator with Integrated ...
M1E-22-051
FDA UDI
GNI Co.,Ltd·08800046006651·
M1E-22-503
FDA UDI
GNI Co.,Ltd·08800046006699·
M1E-22-553
FDA UDI
GNI Co.,Ltd·08800046006705·
M1E-22-031
FDA UDI
GNI Co.,Ltd·08800046006620·
M1E-18-503
FDA UDI
GNI Co.,Ltd·08800046006606·
M1E-22-053
FDA UDI
GNI Co.,Ltd·08800046006682·
M1E-18-331
FDA UDI
GNI Co.,Ltd·08800046006552·
M1E-22-551
FDA UDI
GNI Co.,Ltd·08800046006675·
M1E-18-031
FDA UDI
GNI Co.,Ltd·08800046006538·
M1E-18-301
FDA UDI
GNI Co.,Ltd·08800046006545·
M1E-18-553
FDA UDI
GNI Co.,Ltd·08800046006613·