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

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    Filters Regulation: Us FDA ×

    ACE/FISHER PERCUTANEOUS TRANSFIXING PINS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Sternum Retractor

    FDA UDI
    KOROS U.S.A., INC.·10840199536563·Sternum Spreader Extra Long Arms 22mm Serrated ...

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867523876·Spine Compression Screw, 5.0x22mm

    PATHO DX LATEX AGGLUTINATION STREP B KIT

    FDA 510(k)
    FDA Class 1 ·Microbiology

    COMPUTERIZED ANESTHESIA RECORDING & INFO NETWORK

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MINICAP PREP KITS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CALI·Product code KDI·June 16, 2014

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·October 19, 2010

    ASR UNI FEMORAL IMPL SIZE 55

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·December 17, 2012

    Pipeline Flex Embolization Device

    FDA Enforcement
    Class I ·Ongoing·Micro Therapeutics Inc,·September 15, 2021