BEUDAMED
    18 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    RABBIT ANTISERUM TO HUMAN IGA

    FDA 510(k)
    FDA Class 2 ·Immunology

    DALTON LIFT CHAIR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    BETEC RETRACTABLE SAFETY SYRINGE (5ML)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    RECEPTAL CANISTER 1000 ML CE

    FDA Adverse Event
    Malfunction ·AMSINO MEDICAL CO., LTD.·Product code GCX·May 25, 2012

    RECEPTAL 1.5LITER PE/CE WITH (50/CASE)

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD.·Product code GCX·August 1, 2011

    NON-PVC RECEPT LINER 2000ML/CE(50/CS)

    FDA Adverse Event
    Malfunction ·HOSPIRA, LTD.·Product code GCX·June 21, 2011

    LAMITRODE S8 LEAD

    FDA Adverse Event
    Injury ·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code LGW·October 6, 2010

    NON-PVC RECEPT. LINER 2000ML/CE(50/CS)

    FDA Adverse Event
    Malfunction ·HOSPIRA, LTD.·Product code GCX·June 21, 2011

    NON-PVC RECEPT LINER 2000ML/CE(50/CS)

    FDA Adverse Event
    Malfunction ·HOSPIRA, LTD.·Product code GCX·June 21, 2011

    RECEPTAL 1.5 LITER PE/CE WITH (50/CASE)

    FDA Adverse Event
    Injury ·HOSPIRA LTD.·Product code GCX·November 18, 2010

    RECEPTAL 1 LITER/CE WITH VALVE (50/CAS)

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD.·Product code GCX·June 24, 2011

    RECEPTAL 1 LITER/CE WITH VALVE (50/CAS)

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD.·Product code GCX·June 24, 2011

    HEMOSTAR LONG-TERM HEMODIALYSIS CATHETER 14.5F STANDARD K

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC (BASD)·Product code MSD·March 6, 2014

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·November 9, 2012

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·PURITAN BENNETT CORP·Product code CBK·September 8, 2010

    2.5NM TORQUE LIMITING NUT DRIVER

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HXX·October 28, 2020

    2.5NM TORQUE LIMITING NUT DRIVER

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HXX·January 28, 2020

    Daig Livewire Steerable, Product Number 401932; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026