BEUDAMED
    100 results · 32ms · Sources: EU EUDAMED, US FDA

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    ANDON BLOOD PRESSURE CUFF

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GRANDIO FLOW

    FDA 510(k)
    FDA Class 2 ·Dental

    ITOTAL CRUCIATE RETAINING (CR) KNEE REPLACEMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523143696·L CIMA HXL PS Tibial Insert Sz A 17mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523147144·PS Tibia Insert Trial Size A, 17mm - Left

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523142835·L E-CIMA Vitamin E PS Tibial Insert Sz A 17mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523144730·L UHMWPE PS Tibial Insert Sz A 17mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523172597·PS Tibia Insert Trial with Posterior Pin Relief...

    EXPRESS LD ILIAC / BILIARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code NIO·January 8, 2026

    EXPRESS LD ILIAC / BILIARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code NIO·August 14, 2025

    EXPRESS LD ILIAC / BILIARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code NIO·December 4, 2025

    EXPRESS LD ILIAC / BILIARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code NIO·December 4, 2025

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·July 22, 2015

    EXPRESS LD ILIAC / BILIARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code NIO·November 5, 2025

    EXPRESS LD ILIAC / BILIARY

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NIO·March 25, 2026

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·June 18, 2015

    EXPRESS LD ILIAC / BILIARY

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NIO·November 21, 2024

    EXPRESS LD ILIAC / BILIARY

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NIO·March 6, 2025

    EXPRESS LD ILIAC / BILIARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code NIO·October 29, 2025

    EXPRESS LD ILIAC / BILIARY

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NIO·August 6, 2025