BEUDAMED
    12 results · 24ms · Sources: EU EUDAMED, US FDA

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    Multi-Sideport Catheter Infusion Set

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MULTI-SIDEPORT DUAL CHECK VALVE CATHETER INFUSION SET

    FDA Adverse Event
    Injury ·COOK INC·Product code KRA·April 27, 2022

    MULTI-SIDEPORT DUAL CHECK VALVE CATHETER INFUSION SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·April 11, 2022

    MULTI-SIDEPORT DUAL CHECK VALVE CATHETER INFUSION SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·August 19, 2022

    Bernafon

    FDA UDI
    Bernafon AG·05711584076194·AQ CO7 B 105, 2.4G NFM DPB SABE/MAC DEMO ACCUQ

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515026513·Wylie Renal Vein Ret, 1"w x 4"D

    ADPHARMA OCCLUDE AND OCCLUDE F DENTIN TUBULE AGENT

    FDA 510(k)
    FDA Class 2 ·Dental

    OSTENE CT, AOC CT, OSTEOTENE, CERETENE

    FDA 510(k)
    FDA Unclassified ·Unknown

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 14, 2025

    INOMAX DSIR (DELIVERY SYSTEM)

    FDA Adverse Event
    Other ·IKARIA·Product code MRN·June 17, 2013

    SM204 M-SERIES W/BIG WHEEL

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·June 22, 2011

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    PINGHU WEIFENG MATERIAL TECHNOLOGY·Product code IKX·October 17, 2014