BEUDAMED
    83 results · 65ms · 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 FDA Adverse Event ×

    CUT/COAGULATION HANDPIECE FOR OPEN SURGERY

    FDA Adverse Event
    Malfunction ·PLASMA SURGICAL INC.·Product code GEI·September 6, 2013

    PLASMAJET SURGICAL SYSTEM

    FDA Adverse Event
    Malfunction ·PLASMA SURGICAL INC.·Product code GEI·August 6, 2015

    PLASMAJET CUT/COAGULATION HANDPIECE

    FDA Adverse Event
    Malfunction ·PLASMA SURGICAL INC.·Product code GEI·April 30, 2012

    SINGLE-USE CUT/COAG HANDPIECE FOR OPEN SURGERY

    FDA Adverse Event
    Injury ·PLASMA SURGICAL INC.·Product code GEI·August 21, 2014

    PLASMA JET

    FDA Adverse Event
    Malfunction ·PLASMA SURGICAL INC·Product code GEI·October 31, 2005

    PLASMAJET NEUTRAL PLASMA SURGERY CONSOLE

    FDA Adverse Event
    Malfunction ·PLASMA SURGICAL INC.·Product code GEI·November 1, 2013

    UNKNOWN PLASMABLADE DEVICE

    FDA Adverse Event
    Injury ·MEDTRONIC ADVANCED ENERGY, LLC·Product code GEI·October 17, 2017

    YC-1800

    FDA Adverse Event
    Malfunction ·NIDEK CO. LTD·Product code LXS·April 10, 2018

    UNKNOWN MAE GENERATOR

    FDA Adverse Event
    Injury ·MEDTRONIC ADVANCED ENERGY, LLC·Product code GEI·October 17, 2017

    ERBE APC 2

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·September 27, 2019

    ERBE APC 300

    FDA Adverse Event
    Injury ·ERBE ELECTROMEDIZIN GMBH·Product code GEI·June 25, 2010

    FLOSEAL MATRIX HEMOSTATIC SEALANT

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORP.·Product code LMF·July 2, 2003

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·February 11, 2026

    ENDOWRIST

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·January 10, 2022

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·April 13, 2026

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·April 3, 2026

    DA VINCI SI SURGICAL SYSTEM

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·October 31, 2013

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·April 30, 2026

    ARTHREX ACP TM DOUBLE SYRINGE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 7, 2024

    DA VINCI

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·September 23, 2021