BEUDAMED
    14 results · 27ms · 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.

    SPIDER SYSTEM KOLIBRI CEMENT NEEDLE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526768468·GENUMEDI PSS GREEN II

    EVONOS

    FDA UDI
    Gyrus ACMI, LLC·00821925016552·GOLDMAN SEPARATOR

    ArgenZ HT+ 98x25 ML D3B

    FDA UDI
    ARGEN CORPORATION, THE·D818130402·Dental porcelain/ceramic restoration kit

    EVEREST Spinal System

    FDA UDI
    VB Spine LLC·10888857562318·Rotation Tube

    CONMED 130402

    FDA Adverse Event
    Malfunction ·CONMED CORPORATION·Product code GEI·January 7, 2026

    ARTHROSCOPY PUMP, MODEL A107

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SITE-RITE VISION ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    HANDLE CEV669B DIA 5MM ANG BIPOLAR [MXI/XOM]

    FDA Adverse Event
    Malfunction ·XOMED MICROFRANCE MFG·Product code GEI·April 9, 2014

    CONNECTION SHIELD

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CLEVELAND·Product code KDJ·May 24, 2013

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·September 30, 2014

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIQ·June 16, 2011

    ADULT DUAL HEATED EVAQUA BREATHING CIRCUIT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZE·September 27, 2013

    Veradius Unity with Software Release 2.1- Amobile, diagnostic X-ray imaging and viewing system. . Model Number: 718132

    FDA Enforcement
    Class II ·Ongoing·Philips North America Llc·December 15, 2021