BEUDAMED
    9 results · 29ms · Sources: EU EUDAMED, US FDA

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    Microwave Ablation System

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

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515027985·Spring Wire Retr, #4, 4 tooth blde, 4 1/2"

    VOYAGER NC CORONARY DILATATION CATHETER AND NC TREK RX CORONARY DILATATION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACTIFLO INDWELLING BOWEL CATHETER SYSTEM KIT, MODELS: 32004, 32005, 32006, 32007

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    NC TREK CORONARY DILATATION CATHETER

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code LOX·December 16, 2022

    BELIFU

    FDA Adverse Event
    Injury ·HONG QIANGXING (SHEN ZHEN) ELECTRONICS LIMITED·Product code GZJ·February 10, 2020

    CAD II

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWE·October 17, 2014

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 28, 2011

    PEDIC-SCR-MATR Ø7 PERF L55 TAN

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code NKB·June 21, 2013