BEUDAMED
    9 results · 23ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    KARL STORZ URETERO-RENOSCOPE/URETERSCOPE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    OPERATING CYSTOSCOPE-URETHROSCOPE

    FDA Adverse Event
    Death ·KARL STORZ SE & CO. KG·Product code FGB·March 8, 2023

    ANCHORAGE

    FDA UDI
    Stryker GmbH·07613327171242·Implant Module

    STERILUCENT PSD-85 HYDROGEN PEROXIDE STERILIZER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    AMEDICA DRUG SCREEN THC/COC, OP1300, PPX, OXY, BAR/BZO TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    AIR OPTIX NIGHT & DAY AQUA

    FDA Adverse Event
    Injury ·PT CIBA VISION BATAM·Product code LPM·December 20, 2010

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·July 17, 2014

    LIGASURE IMPACT

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS SHANGHAI MANUFACTURING. LLC·Product code GEI·December 19, 2012

    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