BEUDAMED
    4,244 results · 73ms · 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 ×

    Corin

    FDA UDI
    P3 MEDICAL LIMITED·05051821005502·

    COREVALVE SYSTEM

    FDA Adverse Event
    Death ·MEDTRONIC CORONARY AND STRUCTURAL HEART·Product code NPT·April 24, 2017

    ADAPTA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NVZ·January 6, 2021

    SMART CONTROL NITINOL STENT SYSTEM

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIO·June 29, 2011

    EPIC STENTED PORCINE HEART VALVE W/FLEXFIT SYSTEM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, COSTA RICA LTDA (CVD)·Product code LWR·November 19, 2020

    ROTAREX

    FDA Adverse Event
    Injury ·UNKNOWN·Product code MCW·December 30, 2023

    COREVALVE TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·December 8, 2023

    MICROPULSE P3 PROBE

    FDA Adverse Event
    Injury ·IRDEX CORPORATION·Product code GEX·December 12, 2025

    SGW STORQ .035 300CM ANGLE STD

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DQX·March 30, 2010

    MITRACLIP® SYSTEM CLIP DELIVERY SYSTEM

    FDA Adverse Event
    Death ·ABBOTT MEDICAL·Product code NKM·April 14, 2026

    EDWARDS PASCAL PRECISION

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NKM·October 29, 2025

    MITRACLIP® SYSTEM CLIP DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code NKM·February 22, 2023

    IMPELLA CP

    FDA Adverse Event
    Injury ·ABIOMED, INC.·Product code OZD·August 23, 2024

    COREVALVE SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC CORONARY AND STRUCTURAL HEART·Product code NPT·April 24, 2017

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·February 13, 2017

    WHITESTAR SIGNATURE SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HQC·August 19, 2017

    WHITESTAR SIGNATURE, ACP

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HQC·August 19, 2017

    BD FACSCANTO II

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code OYE·September 17, 2020

    AS VEGA PS TIBIAL PLATEAU CEMENTED T1+

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·November 20, 2020

    POWERFLEX P3 PTA DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V.·Product code LIT·November 8, 2010