BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    PC ECG

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Bernafon

    FDA UDI
    Bernafon AG·05711584050026·PC7 CP, VC PS GR PRECISO 7

    LINEAR ST

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·December 19, 2023

    MONGOOSE ANGIOGRAPHIC CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DIO-DENT 10 DENTAL DIODE LASER

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

    ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAT·August 13, 2018

    MONGOOSE ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Injury ·TOGO MEDIKIT CO.LTD.·Product code DQO·December 15, 2017

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·October 1, 2014

    7.0MM FLEXIBLE MEDULLARY REAMER/FLAT WIRE/385MM

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code HTO·May 29, 2013

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·June 16, 2011