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

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    COAG-A-MATE MAX

    FDA 510(k)
    FDA Class 2 ·Hematology

    Bard® Renal Sheath

    FDA UDI
    C. R. Bard, Inc.·00801741095016·Bard® Renal Sheath

    909 P37,Z5,BE,2L,144",STKR

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828100786·909 P37,Z5,BE,2L,144",STKR

    DISPOSABLE PERFORATORS, JACOBS, HUDSON

    FDA 510(k)
    FDA Class 2 ·Neurology

    Kendall NPWT Incision Management Dressing Kit

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    PIN DRIVER

    FDA UDI
    Gebr. Brasseler GmbH & Co. KG·14053613279168·

    ACCESSORIES

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code DQX·March 20, 2025

    PINNACLE MTL INS NEUT40IDX60OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS·Product code KWA·March 6, 2013

    OCTRODE PERCUTANEOUS LEAD

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION·Product code LGW·February 11, 2011

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MPRI·Product code NVY·August 8, 2014

    ACIST

    FDA Adverse Event
    Malfunction ·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·April 20, 2007

    INDEFLATOR

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code MAV·February 27, 2024

    INDEFLATOR

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code MAV·March 21, 2024

    BARD® RENAL SHEATH

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code LJE·April 8, 2020