BEUDAMED
    22 results · 23ms · Sources: EU EUDAMED, US FDA

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    MECHANICAL WHEELCHAIR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517636386·CoRoent Ant TLIF PEEK, 12x10x30mm 12°

    DULEX

    FDA UDI
    Davol Inc.·00801741011900·Bard Dulex Mesh

    ADVIA Centaur® FOL MCM

    FDA UDI
    Siemens Healthcare Diagnostics Inc.·00630414208671·Folic Acid Master Curve Material - CENTAUR - CONS

    LOCATOR R-Tx

    FDA UDI
    Zest Anchors, LLC·00840481133701·LOCATOR R-Tx Abutment, Keystone Conical, 2mm Cuff

    MEDLINE PVC URETHRAL CATHETER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ADHESIVE EXL-759

    FDA 510(k)
    FDA Class 2 ·Dental

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·January 5, 2022

    M-SERIES

    FDA UDI
    Savaria Concord Lift·10688503001815·Patient Lifter

    LOGIC FEMORAL PS POR RIGHT SZ 2

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·February 10, 2025

    PERI-STRIPS DRY WITH VERITAS COLLAGEN MATRIX (LINEAR CONFIGURATION ULTRA THIN)

    FDA Adverse Event
    Injury ·SYNOVIS SURGICAL INNOVATIONS·Product code FTM·May 20, 2013

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·September 26, 2014

    NI

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HRS·June 2, 2011

    LOGIC CR FEMORAL POR, LEFT, SZ 3.5

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·December 11, 2024

    VENTED HUMIDIFICATION CHAMBER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·February 20, 2013

    ARCHITECT C8000 SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JGS·February 14, 2013

    ARCHITECT C8000 SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JGS·January 3, 2013

    ARCHITECT C8000 SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JGS·January 3, 2013

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 26, 2023

    ICON SERIES CPAP

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZD·February 22, 2015