23 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VENA TECH VENA CAVA FILTER; VENA TECH 30D VENA CAVA FILTER; VENA TECH LP CAVE FILTER
FDA 510(k)
FDA Class 2
·Cardiovascular
CELSITE ACCESS PORT
FDA Adverse Event
Malfunction
·B. BRAUN MEDICAL SAS·Product code LJT·October 23, 2014
MEDRAD® Veris™ 8600 Vital Signs Monitor
FDA UDI
BAYER MEDICAL CARE INC.·00616258009476·" Veris Cannula, Nasal, Divided, Adult, 10 ea
(...
HI-TORQUE PILOT
FDA UDI
ABBOTT VASCULAR INC.·08717648073953·HI-TORQUE PILOT 200 Guide Wire .014 Straight Ti...
Ovation
FDA UDI
Ortho Development Corporation·00822409121236·Narrow Stem Size 8.5 STD
HI-TORQUE PILOT
FDA UDI
ABBOTT VASCULAR INC.·08717648073960·HI-TORQUE PILOT 200 Guide Wire .014 J Tip 3.0 c...
TRACOE MEDICAL GMBH
FDA registration
TRACOE MEDICAL GMBH·12 products·🇩🇪 Germany
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033164457·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033164464·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033164488·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033164440·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033164471·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033164433·
HYDRO2, HS-75
FDA 510(k)
FDA Class 2
·Ophthalmic
HEALTH-PLUS, SANITEX, RELIANCE, POWDER-FREE LATEX EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
ID NOW COVID-19
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH INC.·Product code QJR·December 18, 2020
EON MINI
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 14, 2013
VASOVIEW HEMOPRO EVH SYSTEM
FDA Adverse Event
Injury
·MAQUET CARDIOVASCULAR, LLC·Product code GEI·March 1, 2011
TOTAL ABSCESSION GENERAL DRAINAGE CATHETER
FDA Adverse Event
Malfunction
·ANGIODYNAMICS, INC.·Product code GBX·February 5, 2008
Fredrick's Converse Retractor #5 F/O, Model Number: 01-0485. A fiber optic retractor used in plastic surgery procedures to retract tissue.
FDA Recall
Terminated
·Biomet Microfixation, Inc.·Product code FDG·October 24, 2008