BEUDAMED
    7 results · 20ms · 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 ×

    Vapotherm Aerosol Adapter AAA-2

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    FIRST CHECK HOME DRUG TEST FOR MDMA (ECSTASY)

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    ANCHOR-L LUMBAR CAGE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ONE TOUCH ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code NBW·October 30, 2008

    *

    FDA Adverse Event
    Malfunction ·ANGIODYNAMICS·Product code LJT·August 12, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Death ·MPRI·Product code DTB·July 11, 2013

    Model Number L111, ESSENTIO DR SL MRI Pacemaker

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025