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

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    Aequalis Flex Revive Shoulder System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X1814200·18mm H x 14mm W x 20mm L x 0 degree XLIF

    Integra® Miltex®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780361831·Integra® Miltex® Knapp Iris Scissors, 4-1/8", S...

    Foundation Surgical Interwedge

    FDA UDI
    FOUNDATION SURGICAL GROUP INC·00810141040281·Trial - 18x14x20

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X181420120·18mm H x 14mm W x 20mm L x 12 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X18142080·18mm H x 14mm W x 20mm L x 8 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L181420120·18mm H x 14mm W x 20mm L XLIF Trial 12 degree L...

    LUER-LOK

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMF·March 13, 2026

    SYRINGE 20ML LL TIP CONV PAK

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMF·March 23, 2026

    GC FUJI TEMP

    FDA 510(k)
    FDA Class 2 ·Dental

    VANISHPOINT I.V. CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 17, 2014

    8 FR SHEATH

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DYB·June 14, 2013

    PROGRAMMING SOFTWARE

    FDA Adverse Event
    Malfunction ·CYBERONICS INC·Product code LYJ·July 6, 2011

    LUER-LOK

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMF·February 13, 2026

    LUER-LOK

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMF·February 13, 2026

    CER BIOLOXD OPTION HD 36MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·January 28, 2020

    RINGLOC+ REPLACEMENT RING SZ24

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·January 20, 2020

    CER OPT TYPE 1 TPR SLEVE 0MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·January 28, 2020

    BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·September 10, 2021