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 ×

    130 MODIFIED INTEGRAL FEMORAL COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Polystar HK

    FDA UDI
    Merz Dental GmbH·D7091984408·anteriors; shade C1; mould O 48

    NAMIC DUAL BACKCHECK VALVE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ABBOTT TESTPACK PLUS HCG URINE

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    DURATA STS OPTIM ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·February 28, 2013

    UNKNOWN DEPUY ASR HIP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·January 27, 2011

    REGEN/RNGLC+ MULTI 54MM SZ 23

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·August 6, 2014