BEUDAMED
    12 results · 22ms · 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.
    Filters Regulation: Us FDA ×

    Solo-Dex Fascile Continuous Peripheral Nerve Block Catheter and Needle Kit

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Oticon

    FDA UDI
    Oticon A/S·05707131284327·H11V2 TI, BTE 13 WL 85 TC

    AGC TRADITION KNEE SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304240889·

    TRILOGY ACETABULAR SYSTEM ECCENTRIC LINER

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code LPH·November 17, 2000

    LINEAR ST

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·January 8, 2025

    BIO-RAD VARIANT NBS SICKLE CELL PROGRAM

    FDA 510(k)
    FDA Class 2 ·Hematology

    TRITANIUM PERI-APATITIE ACETABULAR SOLID-BACKED SHELL, TRITANIUM PERI-APATITE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TriVerse Femoral Trial

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215098445·

    PENUMBRA SMART COIL

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code HCG·December 11, 2015

    HEARTWARE® VENTRICULAR ASSIST SYSTEM

    FDA Adverse Event
    Malfunction ·HEARTWARE, INC·Product code DSQ·October 8, 2014

    DEPUY ASR XL FEM IMP SIZE 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 30, 2011

    ASR ACETABULAR CUPS 54

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·June 6, 2013