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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    PURITAN-BENNETT VENTILATOR SYSTEM WITH ET/TRACHEOSTOMY TUBE COMPENSATION, TC, OPTION, MODEL 840

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993071·anteriors; shade A3; mould BM

    FUNDUS PHOTO OPHTHALMIC DIGITAL IMAGING SYSTEM, MODEL CFD-440

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Bashir Plus Endovascular Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    METRX SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code HRX·June 10, 2024

    GREENLIGHT MOXY FIBER OPTIC

    FDA Adverse Event
    Malfunction ·AMS INNOVATIVE CENTER-SAN JOSE·Product code GEX·March 1, 2013

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC MILACA, INC.·Product code LWP·August 8, 2014

    SECURE II MED/SURG BED

    FDA Adverse Event
    Other ·STRYKER MEDICAL·Product code FNL·February 7, 2011

    Daig Livewire Steerable, Product Number 401575; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026