BEUDAMED
    10 results · 35ms · 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.

    ADULT,STERILE,DISPOS.,NONIVAS.,BLOOD PRESS. CUFFS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    3M™ Victory Series™

    FDA UDI
    3M UNITEK CORPORATION·00652221112873·3M™ Victory Series™ Second Molar Bands, 905-147...

    MODIFIED DSL-2300 ACTH RIA

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    JOSLYN STEAM STERILIZER / STEAM MODERNIZATION KIT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BD SYRINGE 5ML LS DN EMERALD

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·December 2, 2021

    ACCENT DR RF

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·January 9, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·November 22, 2010

    EDWARDS ASCENDRA 3 DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code NPT·July 1, 2014

    smiths medical Pneupac paraPAC plus 300 ventilator kit without PEEP and CPAP, REF P300NUS

    FDA Enforcement
    Class I ·Ongoing·Smiths Medical ASD Inc.·March 27, 2024

    paraPAC 300 ventilator kit without internal PEEP and CPAP, Item Number P300N

    FDA Enforcement
    Class I ·Ongoing·Smiths Medical ASD Inc.·October 2, 2024