BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Pantheon Proximal Femur Reconstruction (PFR) System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NATURAL RUBBER LATEX MALE CONDOMS

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    EPI-MAX

    FDA 510(k)
    FDA Unclassified ·Unknown

    CMD 24-1186 HUMERAL STEM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code JDC·August 22, 2024

    CMD 24-1059 PROMADE ELBOW

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A·Product code JDC·December 2, 2025

    STERLING MONORAIL

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code DQY·November 20, 2008

    BARD POLYURETHANE URETERAL CATHETER-CONE TIP

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC.·Product code EYB·August 17, 2011

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 18, 2013

    ALINITY I TOXO IGG REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code LGD·November 18, 2024