BEUDAMED
    10,000 results · 125ms · Sources: EU EUDAMED, US FDA

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    RESTORE PRIME ADVANCED

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO·Product code LGW·January 5, 2009

    GEMSTAR INFUSION PUMP

    FDA Adverse Event
    Injury ·HOSPIRA·Product code FPA·December 7, 2012

    GEMSTAR INFUSION PUMP

    FDA Adverse Event
    Injury ·HOSPIRA·Product code FRN·December 7, 2012

    UNK

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code KWQ·October 22, 2004

    ITREL

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·October 5, 2010

    2.0/1.0 6 HOLE MEDIUM COMPRESSION PLATE

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code JEY·June 29, 2010

    NCP BIPOLAR LEAD

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·February 1, 2002

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code EZW·March 15, 2013

    EON MINI 16-CHANNEL RECHARGEABLE IPG

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 15, 2011

    LEAD MODEL 304

    FDA Adverse Event
    Malfunction ·LIVANOVA USA, INC.·Product code LYJ·August 8, 2019

    ATTUNE CONV FB PS TB TRL SZ5

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code JWH·October 3, 2019

    LEAD MODEL 303-20

    FDA Adverse Event
    Injury ·CYBERONICS INC·Product code LYJ·June 5, 2013

    CORTRAK ENTERAL ACCESS SYSTEM

    FDA Adverse Event
    Injury ·CORPAK MEDSYSTEMS·Product code FPD·June 3, 2009

    EXPEDIUM 6.35 SCREWS

    FDA Adverse Event
    Injury ·DEPUY SYNTHES SPINE·Product code NKB·February 14, 2017

    LEAD MODEL 302

    FDA Adverse Event
    Malfunction ·CYBERONICS - HOUSTON·Product code LYJ·June 6, 2023

    EXPEDIUM 6.35 SET SCREWS

    FDA Adverse Event
    Injury ·DEPUY SYNTHES SPINE·Product code NKB·February 14, 2017

    ACTIVA

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code MHY·September 17, 2014

    PULSE GEN MODEL 105

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·July 2, 2014

    SEALING CAP FOR 5MM TROCARS

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code OKX·October 4, 2017

    DISP.BALLOON TROCAR HASSON CONE 12/100MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code OKX·December 4, 2025