BEUDAMED
    24 results · 50ms · 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 ×

    Livia

    FDA UDI
    LIFE CARE LTD·07290016952025·Livia - Menstrual Pain Relief Device (Full se...

    Livia - flower-pads

    FDA UDI
    LIFE CARE LTD·07290016952506·Livia Flower Pads (Livia - device Accessories ...

    Livia

    FDA UDI
    LIFE CARE LTD·07290016952001·Livia - Menstrual Pain Relief Device (Full se...

    Livia

    FDA UDI
    LIFE CARE LTD·07290016952742·Livia - Menstrual Pain Relief Device (main un...

    Livia USB

    FDA UDI
    LIFE CARE LTD·07290016952735·Livia - USB Cable Sapre part that may be provi...

    Livia Gel Pads

    FDA UDI
    LIFE CARE LTD·07290016952056·Livia Gel Pads (Livia - TENS device Accessories...

    Livia

    FDA UDI
    LIFE CARE LTD·07290016952018·Livia - Menstrual Pain Relief Device (Full se...

    Livia

    FDA UDI
    LIFE CARE LTD·07290016952032·Livia - Menstrual Pain Relief Device (Full se...

    GELSOFT PLUS

    FDA Adverse Event
    Injury ·VASCUTEK LTD·Product code DSY·December 15, 2021

    ASAHI CORSAIR PRO XS

    FDA Adverse Event
    Injury ·ASAHI INTECC CO., LTD.·Product code DQY·November 17, 2025

    ASAHI CORSAIR MICROCATHETER

    FDA Adverse Event
    Injury ·AV-ASAHI·Product code DQY·February 22, 2011

    ADVANIX BILIARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·September 21, 2023

    ITERO ELEMENT 2

    FDA Adverse Event
    Injury ·ALIGN TECHNOLOGY, LTD.·Product code NOF·June 9, 2024

    G7 HARD BEARING INST RING SZ H

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code LPH·May 26, 2020

    CER OPTION TYPE 1 TPR SLEVE -3

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·January 9, 2024

    Defibtech DDP-100 Adult Defibrillation Pads For use with AED Models: Lifeline and Lifeline Auto (DDU-1:XX Series)- Indicated for use on victims of sudden cardiac arrest (SCA)

    FDA Recall
    Open, Classified ·Defibtech, LLC·Product code MKJ·October 14, 2024

    ASAHI CORSAIR PRO XS

    FDA Adverse Event
    Injury ·ASAHI INTECC CO., LTD.·Product code DQY·December 23, 2025

    ASAHI CORSAIR PRO XS

    FDA Adverse Event
    Malfunction ·ASAHI INTECC CO., LTD.·Product code DQY·June 25, 2025

    OXF UNI TIB TRAY SZA LM/RL PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·March 22, 2020

    OXF TWIN-PEG CMNTD FEM MD PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·March 22, 2020