BEUDAMED
    9 results · 22ms · Sources: EU EUDAMED, US FDA

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

    VARIAX

    FDA UDI
    Stryker GmbH·07613327126204·Posterior Lat. Elbow Plate Insert, LEFT

    CD HORIZON SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    QUANTUM CEMENT RESTRICTOR

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·June 19, 2014

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·February 2, 2013

    PIONEER MATTRESS 30"

    FDA Adverse Event
    Malfunction ·STRYKER CORP., MEDICAL DIVISION·Product code IKY·December 9, 2010

    LOGIC TIB INSERT IMPL CRC, SZ 2, 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 10, 2023

    Captus 4000e Thyroid Uptake System, Model Numbers 5430-30151 and 5430-30152 - Product Usage: is intended to be used by trained nuclear Medicine Technologists or Nuclear Medicine Physicians to perform Thyroid Uptake Procedures.

    FDA Enforcement
    Class II ·Terminated·Capintec Inc·April 1, 2020