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

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    Retraxil

    FDA 510(k)
    FDA Unclassified ·Unknown

    Burr

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113097·BURR FOR ALGERBRUSH 1.0MM

    Vu a-POD™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981042127·39x30mm Trial Rasp 10mm 12 deg

    Disposable Medical Nitrile Examination Gloves- Tested for Use with Chemotherapy Drugs

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Vertex Hip Fracture Nailing System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·November 9, 2023

    LAMITRODE 44, 60 CM

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·August 24, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·November 11, 2014

    DEPUY ASR XL FEM IMP SIZE 49

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD.·Product code KXA·July 23, 2013

    Model Number L111, ESSENTIO DR SL MRI Pacemaker

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