BEUDAMED
    8 results · 36ms · Sources: EU EUDAMED, US FDA

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    ORTHOPEDIC DRILL GUIDE

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

    Sporview VH202 BI

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ECHOVIEW / SHIMASONIC DIAGNOSTIC ULTRASOUND DEVICE, MODEL SDU-2200PRO

    FDA 510(k)
    FDA Class 2 ·Radiology

    ONYX, AVM

    FDA Adverse Event
    Injury ·EV3 NEUROVASCULAR·Product code MFE·July 22, 2014

    PINNACLE MTL INS NEUT40IDX60OD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD.-8010379·Product code KWA·June 13, 2014

    FORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·October 13, 2010

    ALTRX NEUT 36IDX62OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·December 13, 2012

    BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026