BEUDAMED
    19 results · 22ms · Sources: EU EUDAMED, US FDA

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    32mm Glenosphere and Humeral Cup

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814695·GENUMEDI SILVER SIZE VI

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123281·K-WIRE - DOUBLE TROCAR 2.0mm DIA x 150mm

    ACDF STAND ALONE CERVICAL

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code OVE·October 8, 2025

    ELI 10 ELECTROCARDIOGRAPH MODEL ELI 10

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CARDIFF ANTERIOR CERVICAL PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACDF STAND ALONE CERVICAL

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code OVE·April 25, 2025

    ACDF STAND ALONE CERVICAL

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code OVE·December 22, 2025

    TPRLOC COCR CMTD STM T1 12.5MM

    FDA Adverse Event
    Death ·BIOMET UK LTD.·Product code JDI·March 23, 2026

    CMK MOD 12/14 SZ202 L130

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LZO·November 24, 2025

    MERGE CARDIO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE SOLUTIONS INC.·Product code LLZ·October 20, 2023

    JUVEDERM

    FDA Adverse Event
    Injury ·UNKNOWN·Product code LMH·October 7, 2008

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·August 4, 2011

    PLUMSET CLAVE PORT CLAVE SET 103IN NDHP

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·June 20, 2013

    ACDF 03.18.118 MECTA-C SA TIPEEK CAGE 18X15X6X7°

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code OVE·May 12, 2023

    REVITAN, DISTAL PART, CURVED, UNCEMENTED, 24/200

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code KWY·July 20, 2023

    ACDF STAND ALONE CERVICAL

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code OVE·June 13, 2025

    CMK MOD 12/14 SZ202 L130

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·January 8, 2026

    Nemio XG, ultrasound system, SSA-590A with version 1.5 software, Toshiba American Medical Systems, Inc., Tusin, CA.

    FDA Recall
    Terminated ·Toshiba American Med Sys Inc·Product code ITX·December 19, 2006