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

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    TRI-COUNT 7

    FDA 510(k)
    FDA Class 2 ·Hematology

    Stern Root Anchor® Mini Female Ti

    FDA UDI
    STERNGOLD DENTAL LLC·00841549106828·The Stern Root AnchorSystem includes the Stern ...

    BEACON TIP TORCON NB ADVANTAGE CATHETER, TORCON NB ADVANTAGE CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PACE 101/PACE 101H, MODEL 3077 SSI TEMPORARY PULSE GENERATOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MEDICAL UNKNOWN

    FDA Adverse Event
    Malfunction ·TELEFLEX·Product code KNX·March 24, 2014

    LINOX SMART SD 65/18

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO KG·Product code LWS·November 7, 2012

    ACCU-CHEK TENDER INFUSION SET

    FDA Adverse Event
    Injury ·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code FPA·September 9, 2010

    BEACON TIP TORCON NB ADVANTAGE ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code DQO·October 10, 2017

    DQO CATHETER, INTRAVASCULAR, DIAGNOSTIC

    FDA Adverse Event
    Injury ·COOK INC·Product code DQO·August 10, 2023

    OPTETRAK Comprehensive Knee System including OPTETRAK RBK PS Tibial Components. NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·October 13, 2021