BEUDAMED
    31 results · 26ms · Sources: EU EUDAMED, US FDA

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    Green Laser Photocoagulator GYC-500

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Reamer Handle - Long

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215057718·

    SA FLOWABLE ADHESIVE

    FDA 510(k)
    FDA Class 2 ·Dental

    REPROCESSED DAIG LIVEWIRE ELECTROPHYSIOLOGY CATHETERS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·June 10, 2020

    EXPRESS SD RENAL/BILIARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 22, 2025

    EXPRESS SD RENAL/BILIARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·September 3, 2025

    EXPRESS SD RENAL/BILIARY

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·January 27, 2025

    EXPRESS SD RENAL/BILIARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 12, 2025

    EXPRESS SD RENAL/BILIARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·May 13, 2026

    MECTACER BIOLOX DELTA CERAMIC BALL HEAD 12/14 Ø 28 SIZE M 0

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·March 31, 2016

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code KRG·June 7, 2013

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·July 7, 2011

    AXSYM RUBELLA IGG ANTIBODY

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code LFX·September 10, 2008

    CD HORIZON® FENESTRATED SCREW SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·September 3, 2024

    EXPRESS SD RENAL/BILIARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·January 22, 2025

    CD HORIZON® SOLERA¿ FENESTRATED SCREW SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO, MED REL·Product code NKB·July 28, 2025

    CD HORIZON® SOLERA¿ FENESTRATED SCREW SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO, MED REL·Product code NKB·July 28, 2025

    CD HORIZON® SOLERA¿ FENESTRATED SCREW SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·April 2, 2025

    CD HORIZON® SOLERA® SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO., HU·Product code NKB·March 20, 2026