23 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HI-TOQUE BALANCE MIDDLEWEIGHT UNIVERSAL GUIDE WIRE WITH HYDROCOAT HYDROPHILIC COATING, #1009659,1009659J, 1009660, 10096
FDA 510(k)
FDA Class 2
·Cardiovascular
Natus
FDA UDI
XLTEK·00382830016414·Natus Quantum Stim Input Cable, 8ft
ID NOW COVID-19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·January 14, 2021
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033520093·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033520048·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033520031·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033520062·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033520055·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033520086·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033520079·
ID NOW COVID-19
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·June 1, 2020
AT WORK DRUG TEST, MODEL 9177T AWT
FDA 510(k)
FDA Class 2
·Clinical Toxicology
SPECIALTY 55 & MULTIFOCAL (METHAFILCON A) SOFT (HYDROPHILIC CONTACT LENSES FOR DAILY WEAR
FDA 510(k)
FDA Class 2
·Ophthalmic
HEALONID GV
FDA Adverse Event
Injury
·PHARMACIA & UPJOHN, FYRISLUND·Product code LZP·December 27, 2001
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code FSA·March 20, 2013
MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·MED-EL ELEKTROMEDIZINISCHE GERAETE, GMBH·Product code MCM·February 4, 2011
SYNCHROMED II
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·March 14, 2008
HEALONID GV
FDA Adverse Event
PHARMACIA & UPJOHN, FYRISLUND·Product code LZP·December 27, 2001
HEALONID GV
FDA Adverse Event
Injury
·PHARMACIA & UPJOHN, FYRISLUND·Product code LZP·December 27, 2001
HEALONID GV
FDA Adverse Event
Injury
·PHARMACIA & UPJOHN, FYRISLUND·Product code LZP·December 28, 2001