BEUDAMED
    11 results · 20ms · 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 ×

    OSTEONICS ECSI HIP STEM SERIES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    N/A

    FDA UDI
    Smith & Nephew, Inc.·00885556600993·MTO SOD PLI TIBIAL REFERENCE AIMER

    everStick®

    FDA UDI
    Gc America Inc.·J0229008361·everStick® COMBI 1 x 8 cm everStickC&B, 1 x 8 c...

    3M™ Unitek™

    FDA UDI
    3M UNITEK CORPORATION·00652221111289·3M™ Unitek™ Bracket Positioning Gauge One, 2.0-...

    BIOSORBPDX BIOABSORBABLE FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    CLEARPOINT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    SNAP-RING FOR 52MM OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWB·December 4, 2007

    BD TRUCOUNT¿ ABSOLUTE COUNTING TUBES

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND COMPANY BD BIOSCIENCES·Product code GKZ·May 20, 2024

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 8, 2015

    PD CYCLER 110 VOLT HOMECHOICEPRO AUTOMATED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·November 17, 2010

    ASR UNI FEMORAL IMPL SIZE 43

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 8, 2013