BEUDAMED
    210 results · 33ms · Sources: EU EUDAMED, US FDA

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    SKINTACT COOL CONTACT ELECTROSURGICAL GROUNDING PLATES

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ERBE

    FDA Adverse Event
    Malfunction ·LEONHARD LANG GMBH·Product code GEI·November 2, 2022

    ERBE

    FDA Adverse Event
    Malfunction ·LEONHARD LANG GMBH·Product code GEI·March 8, 2023

    ERBE

    FDA Adverse Event
    Malfunction ·LEONHARD LANG GMBH·Product code GEI·February 18, 2025

    ERBE

    FDA Adverse Event
    Injury ·LEONHARD LANG GMBH·Product code GEI·July 27, 2022

    SOLIDEA

    FDA UDI
    CALZIFICIO PINELLI SRL·08300496030362·WONDER MODEL MAMAN 140 SHEER, SIZE L, NERO, GRA...

    TriVerse Femoral Component CR

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215100124·

    ASTRONOMER+WITH SLD

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MODIFICATION TO ZEUS SCIENTIFIC, INC., TPO IGG ELISA TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Immunology

    TELECTRONICS 030-362

    FDA Adverse Event
    Injury ·TELECTRONICS PACING SYSTEMS·Product code DTB·May 27, 1997

    TELECTRONICS 030-362

    FDA Adverse Event
    Injury ·TELECTRONICS PACING SYSTEMS·Product code DTB·January 24, 1997

    IOLMASTER

    FDA Adverse Event
    Injury ·CARL ZEISS MEDITEC AG (JENA SITE)·Product code HJO·March 27, 2013

    LIFEPAK 20 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code LDD·March 21, 2011

    PULSE GEN MODEL 102

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·April 16, 2008

    Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x45 mm Catalog Number: 18965045S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.

    FDA Enforcement
    Class II ·Terminated·Stryker GmbH·June 24, 2020

    C21617 DE LIFE SYSTEMS $PHISIO

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·October 24, 2013

    BD PHOENIX¿ NMIC-311

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 19, 2026

    BD PHOENIX¿ NMIC-311

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 19, 2026

    BD PHOENIX¿ NMIC-306

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 28, 2026

    BD PHOENIX¿ NMIC-306

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 14, 2026