BEUDAMED
    10 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 ×

    CYTOPLAST PTFE SUTURE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Optimus Drill Q – 3.7mm 20mm

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215061807·

    Genius Total Knee System

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215023386·

    SENOVA(R) BLOOD GLUCOSE MONITOR

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    FIRST CHOICE & FIRST CHOICE PLUS

    FDA 510(k)
    FDA Class 2 ·Neurology

    Crescendo Meniscal Insert PS 15mm Size 6

    FDA UDI
    AMPLITUDE SAS·03701089525343·

    VENTED AUTOFEED CHAMBER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·April 22, 2013

    TOTALCARE

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·April 21, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·July 10, 2008

    M-VIZION FEMORAL REVISION SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·June 10, 2025