BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    IV Administration Sets

    FDA 510(k)
    FDA Class 2 ·General Hospital

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197071352·Deaver retractor 50mm, ...

    SACRO-ILIAC SCREW SYSTEM SI-JOINT SCREW 10X55

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code OUR·October 8, 2019

    ECLERIS MICROSTAR COLPOSCOPE

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    SPORVIEW STEAM SELF-CONTAINED BIOLOGICAL INDICATOR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    WAVEWRITER ALPHA

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·September 30, 2025

    ERBE VIO 50 C

    FDA Adverse Event
    Other ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·October 1, 2014

    INTERSTIM

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·June 14, 2013

    ACCU-CHEK ® MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·July 21, 2011

    SACRO-ILIAC SCREW SYSTEM SI-JOINT SCREW 10X40

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code OUR·February 5, 2021