BEUDAMED
    2,508 results · 29ms · Sources: EU EUDAMED, US FDA

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    Otoport/Otocheck Carry Case with Printer

    FDA UDI
    OTODYNAMICS LIMITED·05060396170461·

    OZARK TRAIL

    FDA UDI
    Eye Ojo Corp.·00666197776618·

    Phoenix Ultra Chain

    FDA UDI
    PHOENIX ORTHODONTICS INC·05060772895155·U CHAIN OPEN PERFECT PINK SPOOL 15 FEET

    I-FLOW

    FDA Adverse Event
    Malfunction ·BRAUN·Product code FRN·February 22, 2013

    COULTER® LH 750 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·February 4, 2014

    BREAST IMPLANT 400CC

    FDA Adverse Event
    Other ·MENTOR WORLDWIDE LLC·Product code FTR·March 5, 2024

    SURGICAL MESH

    FDA Adverse Event
    Other ·UNK·Product code FTL·March 5, 2024

    BREAST IMPLANT 400CC

    FDA Adverse Event
    Other ·MENTOR WORLDWIDE LLC.·Product code FTR·March 5, 2024

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·June 24, 2010

    DELTA MESH 122X122XX

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS FREIBURG·Product code HRS·May 21, 2012

    ADDPLUS

    FDA Adverse Event
    Injury ·ULRICH GMBH & CO. KG·Product code MQP·March 8, 2019

    TOPCON

    FDA Adverse Event
    Malfunction ·TOPCON MEDICAL SYSTEMS, INC.·Product code NFJ·January 10, 2017

    DJO SURGICAL

    FDA Adverse Event
    Injury ·ENCORE MEDICAL L.P.·Product code KWS·September 16, 2025

    HAMILTON-T1

    FDA Adverse Event
    Malfunction ·HAMILTON MEDICAL AG·Product code CBK·March 7, 2024

    4.5MM PERIPHERAL SCREW - 40MM

    FDA Adverse Event
    Injury ·STRYKER GMBH·Product code KWS·November 29, 2022

    4.5MM PERIPHERAL SCREW - 28MM

    FDA Adverse Event
    Injury ·STRYKER GMBH·Product code KWS·November 30, 2022

    ESSURE

    FDA Adverse Event
    Injury ·BAYER·Product code HHS·July 24, 2015

    BioFire BCID2 Panel, REF RFIT-ASY-0147, For FilmArray Systems, CE, Blood Culture Identification Panel in vitro diagnostic, Rx Only, UDI: (01)00815381020338

    FDA Enforcement
    Class II ·Terminated·BioFire Diagnostics, LLC·June 30, 2021

    HAMILTON-C1

    FDA Adverse Event
    Malfunction ·HAMILTON MEDICAL AG·Product code CBK·May 3, 2024

    HUMERAL CUP - 40MM DIA X 4MM THK

    FDA Adverse Event
    Injury ·STRYKER GMBH·Product code KWS·November 30, 2022