BEUDAMED
    8 results · 29ms · Sources: EU EUDAMED, US FDA

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    Met One Czar Anterior Cervical Plate System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BONEMEDIK-DM

    FDA 510(k)
    FDA Class 2 ·Dental

    MIRAGE MICRO MODEL 16333 (S), 16334 (M&L), 16335 (LW & XL)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    STEM: AMISTEM C CEMENTED STD STEM SIZE 2

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·March 31, 2022

    PELORIS RAPID TISSUE PROCESSOR

    FDA Adverse Event
    Malfunction ·LEICA BIOSYSTEMS MELBOURNE·Product code IEO·October 8, 2014

    SROM STM STD 36+12L 13X18

    FDA Adverse Event
    Malfunction ·DEPUY (IRELAND) - 9616671·Product code LPH·June 20, 2013

    HEMOPRO2 EXTENSION CABLE

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC.·Product code GEI·April 29, 2011

    cobas 6000 Modular Series system; Part Numbers: 1. 04745914001 cobas c 501 module; 2. 05036453001 cobas 6000 UL c 501 + Core Fix configuration; 3. 05036453692 - cobas 6000 UL + CORE CU; and 4. 05860636001 cobas 6000 c 501 (UL) V

    FDA Enforcement
    Class II ·Terminated·Roche Diagnostics Corporation·March 14, 2018