BEUDAMED
    7 results · 37ms · 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.

    OSTEOTECH MUSCULOSKELETAL TISSUE RECOVERY PACK

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00681490907187·INSTRUMENT 8951811 18MM IMP HLDR 18X26MM

    SLIT CAMERA MODEL 07-624

    FDA 510(k)
    FDA Class 1 ·Radiology

    Motor and Apex Module (MaAM)

    FDA 510(k)
    FDA Class 1 ·Dental

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·RICE CREEK MFG·Product code DXY·February 9, 2013

    UNICEL® DXC 800 PRO SYNCHRON® CHEMISTRY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JGS·January 7, 2011

    NATURALYTE

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·July 2, 2014