BEUDAMED
    3,232 results · 25ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    Kangbeier Surgical Mask (Model: KBR-1001)

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

    AUTOMATED IMPELLA CONTROLLER

    FDA Adverse Event
    Malfunction ·ABIOMED, INC.·Product code PYX·July 22, 2025

    DAVIS TONSIL NEEDLE 1/2 CIRCLE

    FDA Adverse Event
    CINCINNATI SURGICAL·Product code KBR·July 30, 1992

    19 G X 1 1/2 IN. BD NOKOR¿ FILTER NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code GAA·August 8, 2017

    BD POSIFLUSH SP

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FOZ·February 25, 2025

    VITEK® 2 AST-P580 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·December 21, 2018

    VITEK® 2 AST-P580 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·December 21, 2018

    BD NEEDLE 25GA 1IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMI·November 30, 2021

    VITEK® 2 GRAM-POSITIVE ANTIMICROBIAL SUSCEPTIBILITY TEST AST-P654 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code LON·March 21, 2019

    VITEK® 2 GRAM-POSITIVE ANTIMICROBIAL SUSCEPTIBILITY TEST AST-P654 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code LON·March 21, 2019

    VITEK® 2 AST-P631 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code LON·July 13, 2018

    VITEK®2 AST-P592 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·August 20, 2018

    INFINITYTM ANTEROMEDIAL GUIDE R 9/10MM

    FDA Adverse Event
    Malfunction ·CONMED CORPORATION·Product code LXH·March 29, 2021

    VITEK® 2 AST-P631

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code LON·March 28, 2018

    GOLD PROBE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·September 11, 2019

    Needle, Tonsil Suturing

    FDA classification
    FDA Class 1 ·Needle, Tonsil Suturing

    CBR ENTERPRISE LIMITED

    FDA registration
    CBR ENTERPRISE LIMITED·358 products·🇭🇰 Hong Kong

    EBR SYSTEMS INC.

    FDA registration
    EBR SYSTEMS INC.·7 products·🇺🇸 United States

    EBR SYSTEMS INC.

    FDA registration
    EBR SYSTEMS INC.·7 products·🇺🇸 United States

    CBR SYSTEMS, INC.

    FDA registration
    CBR SYSTEMS, INC.·1 product·🇺🇸 United States