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

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    NPH-KLENZ

    FDA 510(k)
    FDA Class 1 ·General Hospital

    VARIAX

    FDA UDI
    Stryker GmbH·07613327125757·Olecranon Plate Insert

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·10801902140873·Pediatric Two-Lumen Central Venous Catheterizat...

    INSUFLOW SYNERGY PORT, INSUFLOW SYNERGY XL PORT

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

    LIFECARE 4/HOMECARE - 4H PUMP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    RATCHETING HANDLE WITH QUICK COUPLING

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code LXH·January 5, 2026

    ALLEGRETTO WAVE EYE-Q

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

    ADVANTAGE SERIES 29

    FDA Adverse Event
    Malfunction ·STRYKER CORP., MEDICAL DIV.·Product code FPO·December 9, 2010

    POWERED WHEELCHAIR

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

    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