BEUDAMED
    12 results · 26ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    SAS SHIGELLA BOYDII TYPE 8 ANTISERUM

    FDA 510(k)
    FDA Class 2 ·Microbiology

    SURGISTAR

    FDA UDI
    SURGISTAR, INC.·00878799003706·

    P.F.C. SIGMA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295239505·P.F.C. SIGMA TC3 TIBIAL INSERT TRIAL SZ 4 12.5m...

    De Soutter Medical

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

    VisionAir Enhanced Stock Stent

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    KSEA BIPOLAR ELECTROTOME

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    DRILL 34 MM AO ATTACHMENT

    FDA Adverse Event
    Malfunction ·NEWDEAL S.A.·Product code HTW·November 30, 2006

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·February 14, 2013

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·January 14, 2011

    RESTORE SENSOR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·July 28, 2014

    CONTOUR ACETABULAR RECONSTRUCTION RING

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDJ·June 6, 2025

    MESH, SURGICAL, ACETABULAR, HIP, PROSTHESIS

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDJ·January 23, 2026