BEUDAMED
    107 results · 12ms · Sources: EU EUDAMED, US FDA

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    Maquet Orchide OR Light Systems, Model Numbers and Catalog Numbers OHDII FHD QL VP01 - ARD568803935, OHDII FHD QL AIR03 U - ARD568803952, OHDII FHD QL AIR03 E - ARD568803967, OHDII FHD QL AIR04 E/U - ARD568803968, OHDII FHD QL+ VP01 - ARD569204944, OHDII AIR03 QL FHD E - ARD568803951

    FDA Recall
    Open, Classified ·Getinge Usa Sales Inc·Product code FTD·November 8, 2023

    Brand Name: GlideScope Core 15-inch FHD Model/Catalog Number: 0570-0437 Software Version: Core 15 FHD v1.7 and earlier Product Description: Serialized Monitor

    FDA Recall
    Open, Classified ·Verathon, Inc.·Product code CCW·April 29, 2024

    Mojo Full Face with Headgear, All Sizes

    FDA Recall
    Open, Classified ·SleepNet Corporation·Product code BZD·March 1, 2024

    SystemOne (Q-Series), DreamStation, DreamStation Go, Dorma 400, Dorma 500, REMstar SE Auto Noncontinuous Ventilators The Philips Respironics E30 ventilator is intended to provide invasive and non-invasive ventilatory support for individuals with Respiratory Insufficiency. It is specifically for the care of adult and pediatric patients >7 years of age and >18kgs.

    FDA Recall
    Open, Classified ·Philips Respironics, Inc.·Product code BZD·June 14, 2021

    Magic3 Go Intermittent Urinary Catheters, Female Catalog Numbers: a) REF 51808, b) REF 51810, c) REF 51812, d) REF 51814, e) REF 51816, f) REF 51818

    FDA Recall
    Open, Classified ·C.R. Bard Inc·Product code EZD·April 20, 2023

    DreamStation Auto BiPAP. Non-Continuous Ventilator.

    FDA Recall
    Open, Classified ·Philips Respironics, Inc.·Product code BZD·June 30, 2025

    HydroSil Go Intermittent Urinary Catheters, Catalog Numbers: a) REF 71808, b) REF 71810, c) REF 71812, d) REF 71814, e) REF 71816, f) REF 71818

    FDA Recall
    Open, Classified ·C.R. Bard Inc·Product code EZD·April 20, 2023

    Magic3 Go Intermittent Urinary Catheters, pediatric Catalog Numbers: a) REF 52810G

    FDA Recall
    Open, Classified ·C.R. Bard Inc·Product code EZD·April 20, 2023

    Phantom 2 Nasal Vented Mask

    FDA Recall
    Open, Classified ·SleepNet Corporation·Product code BZD·March 1, 2024

    Philips Respironics DreamWear Full Face Mask

    FDA Recall
    Open, Classified ·Philips Respironics, Inc.·Product code BZD·September 6, 2022

    Therapy Mask 3100 NC/SP

    FDA Recall
    Open, Classified ·Philips Respironics, Inc.·Product code BZD·September 6, 2022

    AirTouch F20 Full Face Mask and User Guide

    FDA Recall
    Open, Classified ·Product code BZD·November 20, 2023

    Mojo 2 Full Face AAV Non Vented Mask, All Sizes

    FDA Recall
    Open, Classified ·SleepNet Corporation·Product code BZD·March 1, 2024

    iQ 2 Nasal Vented Mask

    FDA Recall
    Open, Classified ·SleepNet Corporation·Product code BZD·March 1, 2024

    DreamStation Auto CPAP. Non-Continuous Ventilator.

    FDA Recall
    Open, Classified ·Philips Respironics, Inc.·Product code BZD·June 30, 2025

    Mojo 2 Full Face Vented Mask, All Sizes

    FDA Recall
    Open, Classified ·SleepNet Corporation·Product code BZD·March 1, 2024

    Mojo 2 Full Face Non Vented Mask, All Sizes

    FDA Recall
    Open, Classified ·SleepNet Corporation·Product code BZD·March 1, 2024

    DreamWisp Nasal Mask with Over the Nose Cushion

    FDA Recall
    Open, Classified ·Philips Respironics, Inc.·Product code BZD·September 6, 2022

    Philips DreamStation Auto BiPAP and CPAP, Model Numbers UCDSX500S11, UDSX500S11, UDSX500S11F, UDSX700S11, UDSX700S11F, UFRX500S14. Used to deliver positive airway pressure therapy for the treatment of Obstructive Sleep Apnea.

    FDA Recall
    Open, Classified ·Philips Respironics, Inc.·Product code BZD·February 10, 2023

    AirFit F20 Full Face Mask and User Guide

    FDA Recall
    Open, Classified ·Product code BZD·November 20, 2023