BEUDAMED
    8 results · 24ms · 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.

    BIONECT HYDROGEL

    FDA 510(k)
    FDA Unclassified ·Unknown

    Polystar HK

    FDA UDI
    Merz Dental GmbH·D7091984413·anteriors; shade C1; mould Q 58

    CUSA SYSTEM 200H ULTRASONIC SURGICAL ASPIRATOR

    FDA 510(k)
    FDA Unclassified ·Unknown

    X-RAY TUBE HOUSING ASSEMBLY, VARIOUS MODELS

    FDA 510(k)
    FDA Class 1 ·Radiology

    DURATA STS OPTIM ACTIVE FIXATION, DF4 CONNECTOR

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

    PFC SIGMA/OV/DOME PAT 3PEG,38

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·January 27, 2011

    TILDA T 60 CE

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code NVN·August 6, 2014

    PIPELINE FLEX W/SHIELD TECHNOLOGY

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·August 17, 2020