BEUDAMED
    1,270 results · 27ms · Sources: EU EUDAMED, US FDA

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    NEOMED ORAL/ENTERAL SYRINGE

    FDA Adverse Event
    Malfunction ·NEOMED, INC./AVANOS MEDICAL, INC.·Product code PNR·February 3, 2026

    TX1 TISSUE REMOVAL SYSTEM - CONSOLE

    FDA Adverse Event
    Malfunction ·AOI, INC.·Product code LFL·January 21, 2014

    ABL90 FLEX ANALYZER

    FDA Adverse Event
    Malfunction ·RADIOMETER MEDICAL APS·Product code CHL·April 20, 2018

    MAMMARY IMPLANT

    FDA Adverse Event
    Injury ·DOW CORNING, PNR·Product code FTR·October 10, 1995

    BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BD (SUZHOU)·Product code FOZ·October 29, 2019

    PKG CROSSFIRE 2 CONSOLE

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY-SAN JOSE·Product code GEI·August 15, 2025

    HEARTMATE 3 LEFT VENTRICULAR ASSIST SYSTEM

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·April 6, 2018

    Rexton

    FDA UDI
    Ws Audiology Usa, Inc.·04046355368606·Rexton HA RX DAY 6+ P (NR) BG Hearing Aid

    Rexton

    FDA UDI
    Ws Audiology Usa, Inc.·04046355368613·Rexton HA RX DAY 6+ P (NR) GNT Hearing Aid

    Rexton

    FDA UDI
    Ws Audiology Usa, Inc.·04046355366862·Rexton HA RX BRIDGE 8+ P (NR) BG Hearing Aid

    Rexton

    FDA UDI
    Ws Audiology Usa, Inc.·04046355368316·Rexton HA RX DAY 4+ P (NR) BG Hearing Aid

    MICROFX OCD UNIVERSAL DRILL

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY-SAN JOSE·Product code HTW·June 23, 2017

    HEARTMATE 3 LEFT VENTRICULAR ASSIST SYSTEM

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·August 21, 2018

    UNK KNEE FEMORAL LCS

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·April 12, 2023

    UNK KNEE TIBIAL TRAY LCS

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·April 12, 2023

    UNK KNEE TIBIAL INSERT LCS

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·April 12, 2023

    PROXIMATE*PPH PROCEDURE SET

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·March 11, 2025

    BARDIA® FOLEY CATHETER SILICONE COATED

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZC·August 15, 2022

    BARDIA® FOLEY CATHETER SILICONE COATED

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZC·August 15, 2022

    BD INTIMA-II Y 24GAX0.75IN PRN/EC SLM

    FDA Adverse Event
    Malfunction ·BD SUZHOU (MDS)·Product code FOZ·January 10, 2025