BEUDAMED
    12 results · 19ms · 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 ×

    AeroDVx Arm System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AED

    FDA UDI
    NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.·00848657006477·Handle, round

    Pressure Sentinel®

    FDA UDI
    Zimmer, Inc.·00889024039070·

    Pressure Sentinel®

    FDA UDI
    Zimmer, Inc.·00889024039087·

    200 MICRON TFL SINGLE USE FIBER

    FDA Adverse Event
    Malfunction ·GYRUS ACMI, INC·Product code GEX·December 13, 2022

    VALVULOTOME, RETROGRADE : 03-7500- 03-7510, ANTEGRADE 03-7520

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SIGN PEDIATRIC FIN NAIL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACCESS® TOXO IGG

    FDA Adverse Event
    BECKMAN COULTER, INC.·Product code LGD·February 17, 2012

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 25, 2011

    SYNERGY

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LGW·August 25, 2008

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·July 12, 2013

    ACCOLADE DR SL MRI (Model L311)

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