BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    MODIFIED HCG ENZYME IMMUNOASSAY TEST KIT

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    OXIMETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PATIENT EXAMINATION GLOVES (VINYL)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    UNKNOWN DEPUY FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. ¿ REG. # 8010379·Product code KWA·June 26, 2014

    ISOFLEX LEAD

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·November 10, 2010

    CORE MICRO DRILL

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code DZJ·November 20, 2012

    Alaris System PC Unit Model 8000, a modular infusion pump and monitoring system

    FDA Enforcement
    Class I ·Terminated·CareFusion 303, Inc.·August 12, 2020