BEUDAMED
    8 results · 19ms · 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 ×

    SOF. CARE CUSHION & SOF-CARE CUSHION COVER

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    zensor system

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    STALIF TT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MINICAP TRANSFER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·October 6, 2020

    MINICAP TRANSFER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·January 3, 2023

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·February 12, 2014

    ALL PURPOSE CATHETER

    FDA Adverse Event
    Other ·ANGIOTECH, MEDICAL DEVICE TECHNOLOGIES·Product code DQO·November 21, 2012

    UNIVERSAL DRILL

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code ERL·September 27, 2010