BEUDAMED
    15 results · 42ms · Sources: EU EUDAMED, US FDA

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    G7 Dual Mobility System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RINGLOC-X E1 H/W 56/32MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·April 11, 2025

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962162613·SMALL CERVICAL DILATOR, 7 1/2", SINGLE ENDED, S...

    LCCS

    FDA UDI
    LCCS Products Limited·04895233602215·Single-use RF Cannula

    RANDOX IMMUNOASSAY PREMIUM PLUS CONTROL LEVELS 1,2 AND LEVEL 3 AND IMMUNOASSAY PREMIUM PLUS TRI-LEVEL CONTROL

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    VERTEX RECONSTRUCTION SYSTEM, VERTEX SELECT RECONSTRUCTION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PRECISION NOVI?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·July 22, 2025

    EON MINI

    FDA Adverse Event
    Death ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 30, 2013

    IAB : 7 FR - 30 CC

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code DSP·June 22, 2011

    O2OPTIX

    FDA Adverse Event
    Injury ·PT CIBA VISION BATAM·Product code LPL·September 5, 2008

    SILHOUETTE PARADIGM INFUSION SET

    FDA Adverse Event
    Injury ·UNOMEDICAL A/S·Product code FPA·December 18, 2017

    SILHOUTTE PARADIGM INFUSION SET

    FDA Adverse Event
    Injury ·MEDTRONIC·Product code LZG·September 18, 2017

    HARMONIC HD 1000I SHEARS 36CM SHAFT

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·October 26, 2020

    INJECTOR N35-O

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code ONB·February 18, 2025

    CONNECTOR C35-O

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code ONB·February 18, 2025