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

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    DUAL LUMEN CATHETER FOR CHRONIC VASCULAR ACCESS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    RxSight Insertion Device

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    ACELL MATRISTEM WOUND SHEET

    FDA 510(k)
    FDA Unclassified ·Unknown

    TOTAL ASR ACET IMP SIZE 58

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·June 24, 2014

    CURLIN 6000

    FDA Adverse Event
    Malfunction ·MOOG·Product code FRN·November 1, 2010

    LAMITRODE S8

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·December 28, 2012

    Azurion 7 M20; Catalog numbers: (1) 722079, (2) 722224, (3) 722234, (4) 722282 (OUS ONLY);

    FDA Enforcement
    Class I ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·February 26, 2025