BEUDAMED
    11 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 Status: Malfunction ×

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 13, 2014

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 12, 2011

    TELIGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 8, 2013

    OXFORD UNI KNEE PHASE III 4.0MM DIAM. FEMORAL DRILL

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code HTW·November 20, 2009

    OXFORD MP 04MM DRILL

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code NRA·April 13, 2017

    ENDO GIA

    FDA Adverse Event
    Malfunction ·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·April 20, 2023

    ENDO GIA

    FDA Adverse Event
    Malfunction ·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·April 19, 2023

    ENDO GIA

    FDA Adverse Event
    Malfunction ·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·April 19, 2023

    OXFORD PH3 CEMENTLESS FEM SZ M

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code NRA·June 20, 2025

    ENDO GIA ULTRA

    FDA Adverse Event
    Malfunction ·US SURGICAL PUERTO RICO·Product code GDW·October 19, 2022

    BINAXNOW COVID-19 AG SELF TEST 2CT

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·March 16, 2023