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

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    Filters Regulation: Us FDA ×

    ETEST CHLORAMPHENICAL

    FDA 510(k)
    FDA Class 2 ·Microbiology

    SYSTEM 1E Liquid Chemical Sterilant Processing System

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NIHON KOHDEN BEDSIDE MONITOR, MODEL BSM-6000S SERIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GRANUFLO

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 25, 2014

    CVC KIT: 16 GA X 8 (20 CM)

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code DQY·February 22, 2013

    EON MINI IPG, 16-CHANNEL RECHARGEABLE

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·February 2, 2011

    LIFE SCOPE PT

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·December 26, 2023

    LIFE SCOPE PT

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·December 8, 2023

    BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026