BEUDAMED
    6 results · 51ms · 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.

    Tearaway Product Family

    Basic UDI-DI
    EU MDR · Eu Md Class 2a ·Galt Medical Corp. ·67 devices

    Valved Tearaway Set Product Family

    Basic UDI-DI
    EU MDR · Eu Md Class 2a ·Galt Medical Corp. ·48 devices

    ANGIODYNAMICS / BIOFLO

    FDA Adverse Event
    Injury ·ANGIODYNAMICS·Product code LJS·September 26, 2017

    PHOTODYNAMIC BONE STABILIZATION SYSTEM

    FDA Adverse Event
    Malfunction ·ILLUMINOSS MEDICAL, INC·Product code QAD·October 10, 2018

    FUSION ZILVER BILIARY SELF-EXPANDING METAL STENT

    FDA Adverse Event
    Malfunction ·COOK ENDOSCOPY·Product code FGE·September 4, 2009

    ANGIODYNAMICS / BIOFLO

    FDA Adverse Event
    Malfunction ·ANGIODYNAMICS·Product code LJS·June 9, 2016