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

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    FDA 510(k)
    FDA Class 2 ·General Hospital

    PRO-TOE VO HAMMERTOW IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ELIA CCP, MODEL 14-5515-01; ELIA CCP CONTROL, MODEL 83-1009-01

    FDA 510(k)
    FDA Class 2 ·Immunology

    NY-STA BLACK 2/0 18" (45CM) DS24 VPL

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·May 5, 2026

    UNKNOWN CARDIOVASCULAR ACCESS

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DRE·November 15, 2018

    UNKNOWN CARDIOVASCULAR ACCESS

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DRE·November 16, 2018

    UNKNOWN CARDIOVASCULAR ACCESS

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DRE·November 19, 2018

    UNKNOWN CARDIOVASCULAR ACCESS

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DRE·November 15, 2018

    UNKNOWN CARDIOVASCULAR ACCESS

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DRE·November 19, 2018

    UNKNOWN CARDIOVASCULAR ACCESS

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DRE·November 16, 2018

    UNKNOWN CARDIOVASCULAR ACCESS

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DRE·November 16, 2018

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 23, 2025

    UNKNOWN CARDIOVASCULAR ACCESS

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DRE·November 20, 2018

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013

    UNKNOWN 28MM SYSTEM 12 INSERT 10 DEGREE HOOD

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK·Product code JDI·July 8, 2011

    SOLETRA

    FDA Adverse Event
    Death ·MEDTRONIC NEUROMODULATION·Product code MHY·September 15, 2008

    SUPRAMID BLACK 3/0 (2) 45CM DS19

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·June 13, 2022

    DAFILON 3/0 (2) 100M

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·December 27, 2023

    UNKNOWN SMF STEM

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDI·May 5, 2020

    UNKNOWN SMF STEM

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDI·May 5, 2020