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

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    FERRIS POLYMEM SILVER WOUND DRESSING

    FDA 510(k)
    FDA Unclassified ·Unknown

    IMPACT-20

    FDA UDI
    Denplus Inc·D8451031307·IMPACT-20, MDP, 11.3 kg

    CONTINUUM KNEE SYSTEM-PS FEMORAL COMPONENTS- POROUS, MODEL XX-YYY-ZZZZZ

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OMEGATRAC, MODEL Z105

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    PROSIMA PELVIC FLOOR REPAIR KIT

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code OTP·April 2, 2013

    CARDIOVASCULAR PROCEDURE KIT

    FDA Adverse Event
    TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTR·March 16, 2011

    KERRISON RONGEUR- 40 DEGREE FWD-3MM

    FDA Adverse Event
    Malfunction ·ABBOTT SPINE, INC.·Product code HTX·April 18, 2008

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 12, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 2, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

    Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x35 mm Catalog Number: 18965035S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.

    FDA Enforcement
    Class II ·Terminated·Stryker GmbH·June 24, 2020

    BD PHOENIX¿ PMIC/ID-107

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·September 4, 2025

    BD PHOENIX¿ PMIC/ID-107

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·July 23, 2025

    BD PHOENIX¿ PMIC/ID-107

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·September 4, 2025