31 results
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24ms
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Sources: EU EUDAMED, US FDA
VISUALINE II (ALSO KNOWN AS SUNLINE) AMPHETAMINE ASSAY
FDA 510(k)
FDA Class 2
·Clinical Toxicology
STRYKER LEIBINGER GMBH & CO. KG
FDA registration
STRYKER LEIBINGER GMBH & CO. KG·76 products·🇩🇪 Germany
BONE SOURCE, HA CEMENT, 10 GM
FDA Adverse Event
Injury
·HOWMEDICA INC.·Product code GXP·July 18, 1997
BONE SOURCE, HA CEMENT, 25 GM
FDA Adverse Event
Injury
·HOWMEDICA INC.·Product code LOD·July 18, 1997
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033104415·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033104385·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033104392·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033104378·
TiWAVE L Lumbar Cage System
FDA UDI
Kalitec Direct LLC·B07323K0101070·Distractor, Smooth Paddle, Lordotic, 7mm
InTess Lumbar Cage
FDA UDI
Kalitec Direct LLC·B07312K0101070·Distractor, Smooth Paddle, 7mm
TiWAVE L Lumbar Cage System
FDA UDI
Kalitec Direct LLC·B07323K0101170·Distractor, Smooth Paddle, Lordotic, 17mm
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033104361·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033104408·
Biosteon® Screw
FDA UDI
BIOCOMPOSITES LTD·15060155710317·The Biosteon® ACL Screw is a cannulated single-...
RENEGADE HI-FLO MICROCATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
PP-CAP EIA FOR THE DETECTION OF IGA ANTIBODIES TO H. PYLORI
FDA 510(k)
FDA Class 1
·Microbiology
8010177-1996-00015
FDA Adverse Event
Malfunction
·Product code HXX·November 26, 1996
DISTRACTION ROD FOR 18MM FRAME, L
FDA Adverse Event
Injury
·HOWMEDICA INC·Product code JEY·December 18, 1997
L-PLATE, 100 DEGREE, 2MM BAR, RIGHT, GSP, 5 HOLE
FDA Adverse Event
Injury
·STRYKER OSTEOSYNTHESIS FREIBURG·Product code HRS·October 23, 2007
6.0MM ROD 500MM
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code NKB·March 19, 2013