BEUDAMED
    12 results · 22ms · 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.
    Filters Regulation: Us FDA ×

    EVOS Small Fragment Upper Extremity Plates

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    inCoris ZI

    FDA UDI
    SIRONA Dental Systems GmbH·E27661732932·inCoris ZI 65/25 F1 1Stück/pcs.

    TRABIS [K173893]

    FDA Adverse Event
    Injury ·COLIGNE AG·Product code PLR·April 23, 2019

    DURETTE IMPLANT

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    PASTELLE Q-SWITCHED ND: YAG LASER

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    SLEEPSTYLE AUTO

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZD·January 2, 2025

    SLEEPSTYLE AUTO

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZD·February 18, 2025

    SLEEPSTYLE AUTO

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZD·September 12, 2024

    SLEEPSTYLE AUTO

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZD·November 14, 2024

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·October 15, 2014

    LIFEVEST WCD 3100 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·June 7, 2013

    EASYTRAK 2

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code OJX·July 23, 2011