BEUDAMED
    33 results · 21ms · Sources: EU EUDAMED, US FDA

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    SONOSITE HAND-CARRIED ULTRASOUND SYSTEM (C1 SERIES)

    FDA 510(k)
    FDA Class 2 ·Radiology

    JOBST forMen

    FDA UDI
    BSN MEDICAL, INC.·04042809849004·FOR MEN 15-20 MM HG KNEE HIGH CLOSED TOE EXTRA ...

    OLEEVA FOAM

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    DRI ECSTASY URINE CALIBRATORS

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    CAPSTONE SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·May 1, 2018

    BD PHOENIX¿ SMIC-101

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 13, 2026

    CAPSTONE SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MSD DEGGENDORF MFG·Product code MAX·April 19, 2018

    T25 STARDRIVE SHAFT F/MATRIX LONG

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code HXX·April 11, 2013

    HICKMAN 9 FR DUAL-LUMEN CV CATHETER, PEEL-APART INTRODUCER K

    FDA Adverse Event
    Malfunction ·C. R. BARD, INC. (BASD)·Product code LJS·March 1, 2011

    1000ML 0.9% SODIUM CHLORIDE INJECTION USP

    FDA Adverse Event
    Malfunction ·BAXTER·Product code KPE·May 6, 2008

    BD PHOENIX¿ SMIC/ID-101

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·October 16, 2024

    TWINFIX ULTRA PLLA HA 5.5MM W/ NEEDLES- Absorbable Suture anchor Product Number: 72202616

    FDA Enforcement
    Class II ·Ongoing·Smith & Nephew, Inc.·October 28, 2020

    BD PHOENIX¿ SMIC/ID-101

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·July 1, 2024

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC.·Product code NQP·September 7, 2012

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code NQP·July 6, 2012

    VERCISE CARTESIA

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code NHL·October 3, 2022

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC.·Product code NQP·July 6, 2012

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code NQP·July 6, 2012

    BD PHOENIX¿ SMIC-101

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·July 28, 2025

    BD PHOENIX¿ SMIC-101

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·July 28, 2025