BEUDAMED
    89 results · 11ms · Sources: EU EUDAMED, US FDA

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    BYTE Aligner System REF PRS-0063 BYTE All-Day Aligner System BYTE AT-Night Aligner System A custom-made orthodontic appliance, typically supplied in series intended to be worn in succession and self-changed every few weeks, designed to influence the shape and/or function of the stomatognathic system to correct malocclusions.

    FDA Recall
    Open, Classified ·Straight Smile, LLC·Product code NXC·November 4, 2024

    Centered Glenosphere w/Screw, CoCr/TA6V/TiN 10-degrees Tilt 32 mm, REF: 115-3210

    FDA Recall
    Open, Classified ·FX SHOULDER·Product code PHX·August 8, 2023

    HeartWare Ventricular Assist System (HVAD), US product: Model No.: 1103; and International Product: Model No.: 1104XX. Product Usage: For use as a bridge-to-cardiac transplantation in patients who are at risk of death from refractory end-stage left ventricular heart failure. Designed for in-hospital and out-of-hospital settings, including transportation via fix-wing aircraft or helicopter.

    FDA Recall
    Open, Classified ·HeartWare, Inc·Product code DSQ·August 17, 2016

    HeartWare HVAD System Controller The HeartWare Ventricular Assist System (VAS is indicated for use as a bridge-to-cardiac transplantation in patients who are at risk of death from refractory end-stage left ventricular heart failure. The HeartWare Ventricular Assist System (VAS) is designed for in-hospital and out-of-hospital settings, including transportation via fix-wing aircraft or helicopter

    FDA Recall
    Open, Classified ·Heartware·Product code DSQ·February 3, 2017

    daVinci Harmonic ACE Curved Shears

    FDA Recall
    Open, Classified ·Intuitive Surgical, Inc.·Product code NAY·January 16, 2019

    Virus Counter Platform with Model Name VC3100

    FDA Recall
    Open, Classified ·Sartorius Corporation·Product code REQ·March 11, 2022

    Scorpion Portal Vein Access Set - Product Usage: used to gain access to the hepatic vein and guide a sharp puncture tool (0.040 Stylet or 17ga Needle) through the parenchyma.

    FDA Recall
    Open, Classified ·Argon Medical Devices, Inc·Product code DYB·July 8, 2021

    Titan 0-Deg Scrotal 20 Cm, Catalog Number ES89202400; inflatable penile Prosthesis

    FDA Recall
    Open, Classified ·Coloplast Manufacturing US, LLC·Product code FHW·March 1, 2023

    Titan Touch NB Scrot Zero 18cm, Catalog Number EN29182400; inflatable penile Prosthesis

    FDA Recall
    Open, Classified ·Coloplast Manufacturing US, LLC·Product code FHW·March 1, 2023

    Titan 0-Deg Infrapubic 20 Cm, Catalog Number ES88202400; inflatable penile Prosthesis

    FDA Recall
    Open, Classified ·Coloplast Manufacturing US, LLC·Product code FHW·March 1, 2023

    Titan Touch NB Infr Zero 16cm, Catalog Number EN28162400; inflatable penile Prosthesis

    FDA Recall
    Open, Classified ·Coloplast Manufacturing US, LLC·Product code FHW·March 1, 2023

    Titan 0-Deg Scrotal 18 Cm, Catalog Number ES89182400; inflatable penile Prosthesis

    FDA Recall
    Open, Classified ·Coloplast Manufacturing US, LLC·Product code FHW·March 1, 2023

    Titan NB Infra Zero Ang 16cm, Catalog Number EN88162400; inflatable penile Prosthesis

    FDA Recall
    Open, Classified ·Coloplast Manufacturing US, LLC·Product code FHW·March 1, 2023

    Titan Pump Assembly, Catalog Number 5177701400; inflatable penile Prosthesis

    FDA Recall
    Open, Classified ·Coloplast Manufacturing US, LLC·Product code FHW·March 1, 2023

    Titan Touch Infr Zero Ang 22cm, Catalog Number ES28222400; inflatable penile Prosthesis

    FDA Recall
    Open, Classified ·Coloplast Manufacturing US, LLC·Product code FHW·March 1, 2023

    Titan Touch Infr Zero Ang 18cm, Catalog Number ES28182400; inflatable penile Prosthesis

    FDA Recall
    Open, Classified ·Coloplast Manufacturing US, LLC·Product code FHW·March 1, 2023

    Titan Touch NB Infr Zero 18cm, Catalog Number EN28182400; inflatable penile Prosthesis

    FDA Recall
    Open, Classified ·Coloplast Manufacturing US, LLC·Product code FHW·March 1, 2023

    Titan Touch NB Scrot Zero 16cm, Catalog Number EN29162400; inflatable penile Prosthesis

    FDA Recall
    Open, Classified ·Coloplast Manufacturing US, LLC·Product code FHW·March 1, 2023

    Titan Touch Scro Zero Ang 20cm, Catalog Number ES29202400; inflatable penile Prosthesis

    FDA Recall
    Open, Classified ·Coloplast Manufacturing US, LLC·Product code FHW·March 1, 2023

    Titan Touch Scro Zero Ang 16cm, Catalog Number ES29162400; inflatable penile Prosthesis

    FDA Recall
    Open, Classified ·Coloplast Manufacturing US, LLC·Product code FHW·March 1, 2023