BEUDAMED
    12 results · 21ms · Sources: EU EUDAMED, US FDA

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    Fitmore Hip Stem

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    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

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

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

    CMK MOD 12/14 SZ202 L130

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

    BD INSYTE AUTOGUARD

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY·Product code FOZ·October 27, 2023

    HOVERTRANS TRANSFORMER WITH POWER DRIVE MODEL HTT-650P

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    E.COLI/P. AERUGINOSA PNA FISH

    FDA 510(k)
    FDA Class 1 ·Microbiology

    MERGE CARDIO

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

    STAPLE, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·October 22, 2014

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 20, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 4, 2011