BEUDAMED
    7 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 ×

    SCUBA SYSTEM

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    A.B. DENTAL DEVICES Dental Implants System

    FDA 510(k)
    FDA Class 2 ·Dental

    VENTED VIAL ADAPTER TRANSFER DEVICE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    EDWARDS SAPIEN 3 TRANSCATHETER HEATH VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·September 20, 2018

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·February 14, 2013

    SIG PS CEM FEM W/LUGS LT SZ3

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·January 7, 2011

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·July 29, 2014