BEUDAMED
    9 results · 18ms · Sources: EU EUDAMED, US FDA

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    SONICATOR 720 (MODEL ME720)

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    FEMORAL HEAD BIOLOX DELTA CERAMIC 12/14 - 36 S

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code LZO·June 20, 2022

    DYNASTY® A-CLASS® STD POLY LINER 36MM GROUP G

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code JDI·June 20, 2022

    VARIOUS SUPPORTS AND SPLINTS

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    Catalyst CSR 3 Peg Glenoids

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VITALITY 2

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 19, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 27, 2014

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·December 14, 2012

    BW Lasso 2515 ANV eco Variable Diagnostic EP Catheter, REF D134301 Diagnostic electrophysiology (EP) catheters are specially designed electrode catheters that transmit electrical impulses and can be positioned for endocardial recording or stimulation.

    FDA Enforcement
    Class II ·Terminated·Stryker Sustainability Solutions·January 30, 2019