BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    XPERT MRSA/SA SSTI ASSAY

    FDA 510(k)
    FDA Class 2 ·Microbiology

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810014607788·STERIS-AMSCO 1080/2080 W/LEG EXTENSION 3.25" SO...

    AVISTA MRI

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·May 11, 2024

    PUMA DENTAL CHAIR AND UNIT

    FDA 510(k)
    FDA Class 1 ·Dental

    HANDMASTER

    FDA 510(k)
    FDA Class 2 ·Neurology

    ZILVER FLEX 35 BILIARY SELF-EXPANDING STENT

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FGE·February 24, 2017

    ZILVER FLEX 35 BILIARY SELF-EXPANDING STENT

    FDA Adverse Event
    Malfunction ·COOK INC·Product code NIO·July 25, 2017

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·April 12, 2013

    ACCESS® 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code MMI·May 6, 2011

    ARTHROCARE/OPUS

    FDA Adverse Event
    Malfunction ·ARTHROCARE·Product code GEI·July 23, 2008

    VIVA QUAD XT CRT-D

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code NIK·February 9, 2026