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

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    Celerity Chemical Indicator for enspire 3000 CLCSPS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MaXcess

    FDA UDI
    Nuvasive, Inc.·00887517196613·MaXcess 4 Set Screw, Long

    IMPACTOR TIP

    FDA UDI
    Osteocentric Technologies, Inc.·00810189110519·IMPACTOR TIP

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694007528·Hemi Mesh, Right Mandible/Left Maxilla, 11mm

    NA

    FDA UDI
    aap Implantate AG·04042409038228·Screwdriver cannulated CS 6.5/7.5, hexagonal, ø...

    CENTRAL STATION, VERSION 3.3H

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ReWalk P6.0

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    TANDEM T:SLIM DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE INC.·Product code LZG·October 29, 2014

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 8, 2011

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·July 22, 2013

    AMPLATZER VASCULAR PLUG II

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code KRD·July 28, 2023

    BD ULTRASAFE PASSIVE¿ X-SERIES NEEDLE GUARD SYRINGE - X100L

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON HUNGARY KFT (BD)·Product code MEG·November 17, 2022

    BELLATEK HYBRID BAR 4 IMPLANTS

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code NHA·December 26, 2024

    BELLATEK HYBRID BAR 4 IMPLANTS

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code NHA·January 6, 2025

    BELLATEK¿ HYBRID BAR 5 IMPLANTS

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code NHA·February 18, 2025

    BELLATEK HYBRID BAR 5 IMPLANTS

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code NHA·March 18, 2025

    BELLATEK HYBRID BAR 4 IMPLANTS

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code NHA·January 6, 2025