10,000 results
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53ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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IL TEST FREE PROTEIN S
FDA 510(k)
FDA Class 2
·Hematology
DEPUY INTL., LTD.
FDA registration
DEPUY INTL., LTD.·74 products·🇬🇧 United Kingdom
JOE FRESH
FDA UDI
FGX INTERNATIONAL INC.·00193033182628·
JOE FRESH
FDA UDI
FGX INTERNATIONAL INC.·00193033182604·
neoWave LS
FDA UDI
XENIX MEDICAL LLC·00818345024045·Paddle Shaver, 9mm
JOE FRESH
FDA UDI
FGX INTERNATIONAL INC.·00193033182642·
JOE FRESH
FDA UDI
FGX INTERNATIONAL INC.·00193033182611·
JOE FRESH
FDA UDI
FGX INTERNATIONAL INC.·00193033182635·
InTess Lumbar Cage
FDA UDI
Kalitec Direct LLC·B07312K0103090·Shaver, Closed, 9mm
MODOFICATION TO AFFFINITY 38 MICRO ARTERIAL BLOOD FILTER WITH CARMEDA BIOACTIVE SURFACE, MODELS CB351/CB352
FDA 510(k)
FDA Class 2
·Cardiovascular
INSTANT-VIEW MORPHINE (2000) URINE DIP STRIP TEST
FDA 510(k)
FDA Class 2
·Clinical Toxicology
ASPHERE M SPEC 11/13 36 +3
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·March 14, 2013
PINNACLE MTL INS NEUT36IDX52OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·April 9, 2013
BD MAX¿ ENTERIC BACTERIAL PANEL
FDA Adverse Event
Malfunction
·GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)·Product code PCI·March 8, 2023
PINNACLE MTL INS NEUT40IDX58OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code KWA·September 26, 2012
12/14 ARTICUL 40MM M SPEC+1.5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·September 26, 2012
12/14 ARTICUL 40MM M SPEC+1.5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·September 26, 2012
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC., USA·Product code LFR·May 11, 2007
ARTICULEZE M HEAD 36MM -2
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code JDI·March 19, 2013
V500, SAVINA AND VENTILATORS OF EVITA FAMILY
FDA Adverse Event
Other
·DRAGER MEDICAL GMBH·Product code CBK·February 18, 2011