BEUDAMED
    13 results · 20ms · Sources: EU EUDAMED, US FDA

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    BeneVision N Series Patient Monitors (Including BeneVision N12, BeneVision N15, BeneVision N17, BeneVision N19. BeneVision N22, BeneVision N1)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SSW CARBIDE

    FDA UDI
    Ss White Burs, Inc.·D6901820752·GREAT WHITE GOLD CARBIDE GWSL 6 ROUND - 5 PACK

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515026551·Harrington Splan Ret, #1, 1 1/2"wd, 5" dp, 12 1/2"

    VITEK 2 STRPTOCOCCUS AMPICILLIN

    FDA 510(k)
    FDA Class 2 ·Microbiology

    HANSEN MEDICAL DILATOR FOR ARTISAN CONTROL CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ADVIA CENTAUR XP

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code JJE·October 17, 2014

    PULSE GEN MODEL 101

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·June 21, 2013

    SM104 M-SERIES W/5TH WHEEL

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

    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

    GMK-SPHERE 02.12.0003L FEMORAL COMPONENT SPHERE CEMENTED SIZE 3 L

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·October 14, 2021

    STARDRIVE SCREWDRIVER SHAFT T4/42MM/SELF-RETAINING

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code HXX·March 3, 2016