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

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    SAS SHIGELLA BOYDII TYPE 9 ANTISERUM

    FDA 510(k)
    FDA Class 2 ·Microbiology

    P.F.C. SIGMA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295239529·P.F.C. SIGMA TC3 TIBIAL INSERT TRIAL SZ 4 17.5m...

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471149830·K-WIRE - DOUBLE TROCAR FULLY THREADED 1.5mm DIA...

    SOLARO 3

    FDA 510(k)
    FDA Class 2 ·Dental

    CARDIOMAX-II

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EFB·February 15, 2023

    TERUMO ADVANCE PERFUSION SYSTEM 1

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEM CORP·Product code DTQ·February 11, 2013

    COBAS INTEGRA 800

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·January 14, 2011

    SCREW

    FDA Adverse Event
    Injury ·Product code HWC·July 28, 2014

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EFB·July 26, 2024

    NSK

    FDA Adverse Event
    Malfunction ·NAKANISHI INC.·Product code EFB·September 17, 2025

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EFB·February 18, 2019

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EFB·February 18, 2019

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EFB·February 18, 2019