BEUDAMED
    7 results · 42ms · 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.

    ULTIMA AND ULTIMA LX CEMENTED FEMORAL STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DIMENSION VISTA PROTEIN 3 CALIBRATOR, 3 CONTROL,1 CONTROL L, 1 CONTROL M, 1 CONTROL H

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Galaxy R Digital Radiography Upgrade

    FDA 510(k)
    FDA Class 2 ·Radiology

    DATASCOPE MR MONITOR

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP./PT MONITORING DIVISION·Product code MHX·January 23, 2003

    ASR ACETABULAR IMPLANT 62

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·February 21, 2013

    DXTEND GLENOSPHERE STD D38MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code HSD·January 26, 2011

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 1, 2014