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

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    K-ASSAY HAPTOGLOBIN

    FDA 510(k)
    FDA Class 2 ·Immunology

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993480·anteriors; shade D3; mould ITS

    CUATTRO UNOMD

    FDA 510(k)
    FDA Class 2 ·Radiology

    BIOEASY Multi-Drug Test Cup

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    LEAD EXTRACTION BYRD POLYPROPYLENE EXTRA LONG DILATOR SHEATH SET

    FDA Adverse Event
    Injury ·COOK VANDERGRIFT INC·Product code GCC·January 22, 2021

    ORTHOMET(R) COBALT CHROME FEMORAL HEAD

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LZO·March 7, 2013

    ENDOPATH** XCEL* TROCAR

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·February 16, 2011

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code KRG·August 8, 2014

    LEAD EXTRACTION BYRD POLYPROPYLENE DILATOR SHEATH SET

    FDA Adverse Event
    Malfunction ·COOK VANDERGRIFT INC·Product code GCC·March 9, 2022

    Presource Procedure Packs containing AAMI Level 3 surgical gowns, Multiple Catalog Numbers Produced Between September 1, 2018 and January 15, 2020

    FDA Enforcement
    Class II ·Terminated·Cardinal Health 200, LLC·February 26, 2020