BEUDAMED
    7 results · 18ms · 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 ×

    FRIOS BONESHIELD

    FDA 510(k)
    FDA Class 2 ·Dental

    PTI HEART-CHILL POUCH/PAD SLING (STERILE)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DRX-Revolution Nano Mobile X-ray System

    FDA 510(k)
    FDA Class 2 ·Radiology

    F-R BANDS,30 PROCEDURE

    FDA Adverse Event
    Malfunction ·GYRUS ACMI, INC.·Product code KNH·September 27, 2022

    MYOSURE HYSTEROSCOPIC TISSUE REMOVAL SYSTEM

    FDA Adverse Event
    Injury ·HOLOGIC·Product code HIH·February 15, 2013

    AUTOMATED PD SET W/CASSETTE4 PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·January 31, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 1, 2014