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

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    RANEY CLIP

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    DPS-3300 MICRO NUCLEAR MEDICINE IMAGING COMPUTER

    FDA 510(k)
    FDA Class 2 ·Radiology

    TRIGLYCERIDE'S TEST (TRIGLI-CINET)

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    2.0/2.4MM CRUCIFORM SCRWDRVR BLD/SL-RETAINNG W/HEX COUPLING

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HXX·August 14, 2024

    LOCKING TITANIUM ADAPTER

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·April 18, 2018

    APTIMA MULTITEST SWAB SPECIMEN COLLECTION KIT

    FDA Adverse Event
    Injury ·HOLOGIC, INC.·Product code LIO·August 9, 2024

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 19, 2014

    PINN MAR NEUT 36IDX56OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·October 22, 2010

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Malfunction ·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·December 3, 2012

    GE Healthcare, CARESCAPE Monitor B850, B650 or B450. Patient Monitor.

    FDA Enforcement
    Class II ·Terminated·GE Healthcare, LLC·July 30, 2014