BEUDAMED
    2,734 results · 23ms · 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 ×

    INTERA 3000

    FDA Adverse Event
    Injury ·INTERA ONCOLOGY, INC·Product code LKK·April 13, 2026

    BATROXOBIN REAGENT

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code JCO·September 5, 2024

    OPTUNE

    FDA Adverse Event
    Injury ·NOVOCURE LTD·Product code NZK·January 13, 2015

    NOVOTTF-100A

    FDA Adverse Event
    Other ·NOVOCURE LTD·Product code NZK·November 22, 2013

    UNK MAMMARY IMPLANT

    FDA Adverse Event
    Death ·UNKNOWN MANUFACTURER·Product code FWM·October 24, 2018

    UNK MAMMARY IMPLANT

    FDA Adverse Event
    Injury ·Product code FWM·October 24, 2018

    ORISE PROKNIFE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 14, 2022

    NOVOTTF-100A

    FDA Adverse Event
    Other ·NOVOCURE LTD·Product code NZK·October 21, 2013

    OPTUNE

    FDA Adverse Event
    Injury ·NOVOCURE LTD.·Product code NZK·May 4, 2016

    ETHICON

    FDA Adverse Event
    Injury ·ETHICON ENDOSURGERY J/J CO·Product code GAG·February 8, 2000

    CHROMIC GUT 1 SUTURE

    FDA Adverse Event
    Malfunction ·ETHICON AJ & J CO.·Product code GAL·July 6, 1995

    CHROMIC GUT 1 SUTURE

    FDA Adverse Event
    Malfunction ·ETHICON AJ & J CO.·Product code GAL·July 6, 1995

    CHROMIC GUT 1 SUTURE

    FDA Adverse Event
    Malfunction ·ETHICON AJ & J CO.·Product code GAL·July 6, 1995

    ETHICON ENDO

    FDA Adverse Event
    Malfunction ·ETHICON J & J CO·Product code GDO·September 11, 2001

    J&J ACETABULAR POLYETHYLENE LINER

    FDA Adverse Event
    Injury ·DEPUY INC. (J & J CO)·Product code JDI·May 19, 2000

    VELOCITY RX

    FDA Adverse Event
    Malfunction ·CORDIS. A J & J CO.·Product code MAF·November 29, 2001

    GYNECARE TVT SECURE

    FDA Adverse Event
    Malfunction ·GYNE CARE / ETHICON J & J CO.·Product code FTL·March 10, 2009

    ETHICON

    FDA Adverse Event
    Other ·ETHICON ENDO-SURGERY, INC. J & J CO·Product code GDT·July 17, 2002

    CODMAN

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF INC. A J & J CO.·Product code HBF·July 26, 2004

    8 G MAMMOMARK

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC. A J & J CO.·Product code NEU·October 20, 2009