BEUDAMED
    8 results · 26ms · Sources: EU EUDAMED, US FDA

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    DCL - SYPHILIS-G ASSAY CATALOG NO. 600-70

    FDA 510(k)
    FDA Class 2 ·Microbiology

    B LOCUS HIGH RES SSP UNITRAY KIT WITH TAQ POLY

    FDA Adverse Event
    Malfunction ·LIFE TECHNOLOGIES CORP.·Product code MZI·January 15, 2014

    SOFCARE PATIENT EXAMINATION GLOVES (LATEX)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·June 26, 2014

    SIGMA STAB XLK INS 4 10MM

    FDA Adverse Event
    Injury ·DEPUY (IRELAND)·Product code JWH·January 4, 2013

    RIATA ACTIVE FIXATION

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

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

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