BEUDAMED
    6 results · 18ms · 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.

    HANDY VIBRO BELT

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    AFFIRM VP SAMPLE COLLECTION SET

    FDA 510(k)
    FDA Class 1 ·Microbiology

    SURECATH PORT ACCESS CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ASR XL TAP SLV ADAP 12/14+2

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 22, 2013

    INSYNC MAXIMO

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code NIK·December 14, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 5, 2014