BEUDAMED
    8 results · 19ms · 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 ×

    STABLEMAPR STEERABLE INTRACARDIAC CATHETERS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981642·anteriors; shade D2 light; mould UL2

    RA-I

    FDA 510(k)
    FDA Class 2 ·Radiology

    B-Laser Atherectomy System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ENDURANT ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·February 27, 2013

    CONICAL REAMER SLEEVE

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·January 12, 2011

    3MM DIAMOND BALL

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HSZ·December 18, 2013

    Femoral Nail, A/R T2 Femur ¿10x320 mm, Product Number 18251032S

    FDA Enforcement
    Class II ·Terminated·Stryker GmbH·July 18, 2018