BEUDAMED
    184 results · 93ms · Sources: EU EUDAMED, US FDA

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    PULSE OXIMETER

    FDA Adverse Event
    Other ·OHMEDA·Product code DQA·April 28, 1997

    FLUOROSCOPIC IMAGE INTENSIFIED SYSTEM

    FDA Adverse Event
    Malfunction ·OEC MEDICAL SYSTEMS, INC.·Product code JAA·April 15, 1997

    SARS-COV-2 IGG

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code QKO·June 26, 2020

    HICKMAN 7 FR DL CVC, PEEL-APART INTRO W/SURECUFF

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code LJS·May 30, 2014

    HEARTMATE MOBILE POWER UNIT, NA

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·June 25, 2021

    THORATEC® HEARTMATE 3¿ SYSTEM CONTROLLER

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·July 17, 2024

    ICL (IMPLANTABLE COLLAMER LENS)

    FDA Adverse Event
    Injury ·STAAR SURGICAL COMPANY·Product code MTA·May 19, 2014

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·February 12, 2014

    INFLATABLE PENILE PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR UROLOGY, INC.·Product code FHW·April 8, 1997

    2.3MM X 18MM LOCKING CORTICAL PEG

    FDA Adverse Event
    Malfunction ·ACUMED, LLC·Product code LXH·July 21, 2022

    2.3MM X 20MM LOCKING CORTICAL PEG

    FDA Adverse Event
    Malfunction ·ACUMED, LLC·Product code LXH·July 21, 2022

    SUREFORM

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code GDW·February 2, 2026

    HEARTMATE 3 SYSTEM CONTROLLER

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·August 11, 2022

    HEARTMATE MOBILE POWER UNIT, EU

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·February 13, 2026

    Brand Name: MEDLINE Product Name: SYR 10ML L/S WHITE LIDO Model/Catalog Number: 91873 Product Description: NON-Sterile syringes without needles for single use Component: No

    FDA Recall
    Open, Classified ·Jiangsu Shenli Medical Production Co., Ltd. No.·Product code FMF·April 5, 2024

    LIBERTY CYCLER SET, SINGLE CONN./EXT. DL

    FDA Adverse Event
    Injury ·ERIKA DE REYNOSA, S.A. DE C.V.·Product code FKX·January 5, 2026

    MENTOR SMOOTH ROUND MODERATE PLUS PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·March 18, 2019

    SPEEDSCREW 6.5MM IMPLANT

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORPORATION·Product code HWC·May 30, 2012

    CENTURION SURGICAL PROCEDURE PAK

    FDA Adverse Event
    Malfunction ·ALCON RESEARCH, LLC - HOUSTON·Product code LRO·December 15, 2022

    BD NOKOR¿ FILTER NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code GAA·August 9, 2023