BEUDAMED
    24 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Open, Classified ×

    MAGNETOM Skyra (DE). Model Number: 10432915. 510(k) Numbers: K101347, K111242, K123510, K133435, K140253, K141977, K142515, K153343, K173592, K202014, K231560.

    FDA Recall
    Open, Classified ·Siemens Medical Solutions USA, Inc·Product code LNH·August 28, 2025

    stryker 3.0MM Neuro Match Head, REF 5820-107-430, used to cut bone and bone cement during neurosurgery

    FDA Recall
    Open, Classified ·Stryker Corporation·Product code HBE·June 28, 2023

    stryker 3.0MM Precision Neuro Match Head, REF 5820-107-530, used to cut bone and bone cement during neurosurgery

    FDA Recall
    Open, Classified ·Stryker Corporation·Product code HBE·June 28, 2023

    Disposable Spetzler-Malis Bipolar forceps, 23CM SLM DISP BAYONET 0.5MM, Catalog Number 6780-230-005

    FDA Recall
    Open, Classified ·Stryker Corporation·Product code GEI·September 11, 2023

    Disposable Spetzler-Malis Bipolar forceps, 18CM SM DISP BAYONET 0.5MM TIP, Catalog Number 6760-180-005

    FDA Recall
    Open, Classified ·Stryker Corporation·Product code GEI·September 11, 2023

    Disposable Spetzler-Malis Bipolar forceps, 18CM IM DISP BAYONET 1.0MM TIP, Catalog Number 6770-180-010

    FDA Recall
    Open, Classified ·Stryker Corporation·Product code GEI·September 11, 2023

    Disposable Spetzler-Malis Bipolar forceps, 18CM SM DISP BAYONET 1.5MM TIP, Catalog Number 6760-180-015

    FDA Recall
    Open, Classified ·Stryker Corporation·Product code GEI·September 11, 2023

    Disposable Spetzler-Malis Bipolar forceps, 20CM SLM DISP BAYONET 1.0MM, Catalog Number 6780-200-010

    FDA Recall
    Open, Classified ·Stryker Corporation·Product code GEI·September 11, 2023

    Disposable Spetzler-Malis Bipolar forceps, 23CM SM DISP BAYONET 0.5MM TIP, Catalog Number 6760-230-005

    FDA Recall
    Open, Classified ·Stryker Corporation·Product code GEI·September 11, 2023

    Disposable Spetzler-Malis Bipolar forceps, 23CM IM DISP BAYONET 0.5MM TIP, Catalog Number 6770-230-005

    FDA Recall
    Open, Classified ·Stryker Corporation·Product code GEI·September 11, 2023

    Disposable Spetzler-Malis Bipolar forceps, 20CM SM DISP BAYONET 0.5MM TIP, Catalog Number 6760-200-005

    FDA Recall
    Open, Classified ·Stryker Corporation·Product code GEI·September 11, 2023

    Disposable Spetzler-Malis Bipolar forceps, 18CM IM DISP BAYONET 1.5MM TIP, Catalog Number 6770-180-015

    FDA Recall
    Open, Classified ·Stryker Corporation·Product code GEI·September 11, 2023

    Disposable Spetzler-Malis Bipolar forceps, 18CM IM DISP BAYONET 0.5MM TIP, Catalog Number 6770-180-005

    FDA Recall
    Open, Classified ·Stryker Corporation·Product code GEI·September 11, 2023

    Disposable Spetzler-Malis Bipolar forceps, 23CM SLM DISP BAYONET 1.0MM, Catalog Number 6780-230-010

    FDA Recall
    Open, Classified ·Stryker Corporation·Product code GEI·September 11, 2023

    Disposable Spetzler-Malis Bipolar forceps, 20CM IM DISP BAYONET 1.5MM TIP, Catalog Number 6770-200-015

    FDA Recall
    Open, Classified ·Stryker Corporation·Product code GEI·September 11, 2023

    Disposable Spetzler-Malis Bipolar forceps, 20CM SLM DISP BAYONET 0.5MM, Catalog Number 6780-200-005

    FDA Recall
    Open, Classified ·Stryker Corporation·Product code GEI·September 11, 2023

    Disposable Spetzler-Malis Bipolar forceps, 20CM IM DISP BAYONET 0.5MM TIP, Catalog Number 6770-200-005

    FDA Recall
    Open, Classified ·Stryker Corporation·Product code GEI·September 11, 2023

    Disposable Spetzler-Malis Bipolar forceps, 23CM SM DISP BAYONET 1.0MM TIP, Catalog Number 6760-230-010

    FDA Recall
    Open, Classified ·Stryker Corporation·Product code GEI·September 11, 2023

    Disposable Spetzler-Malis Bipolar forceps, 23CM IM DISP BAYONET 1.0MM TIP, Catalog Number 6770-230-010

    FDA Recall
    Open, Classified ·Stryker Corporation·Product code GEI·September 11, 2023

    Disposable Spetzler-Malis Bipolar forceps, 23CM SM DISP BAYONET 1.5MM TIP, Catalog Number 6760-230-015

    FDA Recall
    Open, Classified ·Stryker Corporation·Product code GEI·September 11, 2023