BEUDAMED
    7 results · 21ms · 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 Regulation: Us FDA ×

    PISTON SYRINGES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TUBING HOLDER

    FDA 510(k)

    OXYGEN, AIR, VACUUM & NITROUS-OXIDE COUPLERS

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    FRESENIUS DIALYSIS DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·FRESENIUS MEDICAL CARE-NORTH AMERICA·Product code KDI·May 16, 2008

    AC-POWERED ADJUSTABLE HOSPITAL BED, INCLUDING RAILS

    FDA Adverse Event
    Malfunction ·CARROLL HEALTHCARE·Product code FNL·February 5, 2013

    EON IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL -NEUROMODULATION·Product code LGW·December 15, 2010

    UNKNOWN DEPUY HEAD BALL

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·July 18, 2014