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

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    CABOT MEDICAL NIAGRA-TRS THERMAL RETENTION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    na

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00885074087955·FUNNEL 2940171 BONE

    VARIAX

    FDA UDI
    Stryker GmbH·07613327126082·Module - Curved, Straight Plates

    ProSeal™ Injector Plus (Model no. 421050)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MICRODERM, MODEL/VERSION 3.5

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

    TERUMO PERFUSION SYSTEM 8000

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code JOR·December 23, 2010

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 2, 2013

    LAP-BAND AP ADJUSTABLE GASTRIC BANDING SYSTEM (STANDARD)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·March 21, 2014

    THREE PEG PATELLA 38MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·January 7, 2025

    Captus 4000e Thyroid Uptake System, Model Numbers 5430-30151 and 5430-30152 - Product Usage: is intended to be used by trained nuclear Medicine Technologists or Nuclear Medicine Physicians to perform Thyroid Uptake Procedures.

    FDA Enforcement
    Class II ·Terminated·Capintec Inc·April 1, 2020