BEUDAMED
    12 results · 28ms · 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 ×

    IOL INJECTOR SET

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    LINEAR 3-4

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·March 12, 2021

    MEDIVISION I-VIEW PERSONAL VIDEO DISPLAY

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    NEUROGRAPH EVOKED POTENTIAL SYSTEMS (EPS), MODEL EPS-1

    FDA 510(k)
    FDA Class 2 ·Neurology

    RINGLOC RIMCUP SHELL

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code LPH·August 31, 2017

    MIH MOD CUP INSERTER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LXH·August 17, 2017

    ST104 TRANSPORT

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FPO·April 22, 2013

    FLOSEAL HEMOSTATIC MATRIX

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - HAYWARD·Product code LMF·April 27, 2011

    BD LOGIC BLOOD GLUCOSE MONITOR

    FDA Adverse Event
    Other ·NOVA BIOMEDICAL CORPORATION·Product code NBW·July 3, 2008

    STYLE 110 SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·August 3, 2017

    STYLE 110 SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·August 3, 2017

    Belmont Rapid Infuser, a Fluid Management System, Model FMS2000.

    FDA Enforcement
    Class II ·Terminated·Belmont Instrument Corporation·October 24, 2012