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.
    Filters Regulation: Us FDA ×

    DISPOSABLE ENDOSCOPIC RETRIEVAL DEVICE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    RUIKE, MODEL 3331

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Voyant Open Fusion Device

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    UNICEL® DXC 600I SYNCHRON® ACCESS® CLINICAL SYSTEM

    FDA Adverse Event
    Injury ·BECKMAN COULTER·Product code MMI·February 14, 2013

    6 SHOOTER SAEED MULTI-BAND LIGATOR

    FDA Adverse Event
    Injury ·COOK ENDOSCOPY·Product code MND·January 12, 2011

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 29, 2014