47 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Med-link Reusable Blood Pressure Cuff, Med-link Disposable Blood Pressure Cuff
FDA 510(k)
FDA Class 2
·Cardiovascular
LEONE SPA
FDA UDI
LEONE SPA·08033707017813·CALIBRA 1ST MOLAR BANDS n.LR 30
OsteoMed
FDA UDI
OSTEOMED LLC·00845694054959·Cannulated Depth Gauge, 1.5mm/2.0mm
SD CERAMIC COPING FOR QUICK ABUTMENT, LOCKING. MODEL 45301. RD CERAMIC COPING FOR QUICK ABUTMENT, LOCKING, MODEL 45302.
FDA 510(k)
FDA Class 2
·Dental
ABX PENTRA CREATININE 120 CP; ABX PENTRA MULTICAL; ABX PENTRA N CONTROL; ABX PENTRA P CONTROL; ABX PENTRA URINE CONTROL
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Widex
FDA UDI
Widex A/S·05706069975048·WIDEX MOMENT M-CIC-M 330 (Light brown)
Widex
FDA UDI
Widex A/S·05706069975062·WIDEX MOMENT M-CIC-M 330 (Dark brown)
Widex
FDA UDI
Widex A/S·05706069563351·Widex UNIQUE U-CIC-M (Dark brown ) 330
Widex
FDA UDI
Widex A/S·05706069563344·Widex UNIQUE U-CIC-M (Clay brown ) 330
Widex
FDA UDI
Widex A/S·05706069975055·WIDEX MOMENT M-CIC-M 330 (Clay brown)
Widex
FDA UDI
Widex A/S·05706069563337·Widex UNIQUE U-CIC-M (Light beige ) 330
INDIGO SYSTEM ASPIRATION CATHETER 5
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code DXE·November 21, 2016
INDIGO SYSTEM ASPIRATION CATHETER D
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code DXE·February 12, 2019
ACCUDRAIN WITH ANTI-REFLUX VALVE
FDA Adverse Event
Malfunction
·INTEGRA NEUROSCIENCES PR·Product code JXG·September 23, 2016
INDIGO SYSTEM CATD ASPIRATION CATHETER
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code DXE·May 29, 2019
INDIGO SYSTEM CATD ASPIRATION CATHETER
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code DXE·January 17, 2020
INDIGO SYSTEM ASPIRATION CATHETER D
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code DXE·December 7, 2018
INDIGO SYSTEM ASPIRATION CATHETER D
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code QEW·January 29, 2021
INDIGO SYSTEM ASPIRATION CATHETER D
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code DXE·December 10, 2020
PENUMBRA SYSTEM JETD REPERFUSION CATHETER
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code DXE·June 5, 2019