BEUDAMED
    20 results · 33ms · Sources: EU EUDAMED, US FDA

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    ENDOPATH ETS FLEX

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code KOG·November 26, 1997

    INTACS PRESCRIPTION INSERTS

    FDA Adverse Event
    Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·June 20, 2006

    ELEVATOR #301

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code EMJ·March 9, 2016

    IMPAX CV REPORTING

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP·Product code LLZ·February 26, 2013

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·February 25, 2011

    GE OEC 9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS, INC·Product code JAA·February 22, 2008

    ELEVATOR #301

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code EMJ·March 9, 2016

    ELEVATOR #301

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code EMJ·February 9, 2016

    INTACS PRESCRIPTION INSERTS

    FDA Adverse Event
    Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·April 3, 2006

    WA4000 20# N20 CONN

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code GEH·May 28, 2020

    CORTICAL BONE SCREW, ÿ 4X28MM

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code HSB·March 4, 2022

    INTACS CORNEAL IMPLANTS

    FDA Adverse Event
    Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·June 20, 2006

    INTACS PRESCRIPTION INSERTS

    FDA Adverse Event
    Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·April 3, 2006

    LM-900 N2O CE CRYOSURG SY

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code GEH·June 7, 2021

    PENUMBRA SYSTEM RED 72 REPERFUSION CATHETER

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·April 8, 2024

    STERNALOCK BLU SYSTEM SCREW, CANCELLOUS CROSS-DRIVE LOCKING 2.4 X 16MM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HRS·February 15, 2019

    STERNALOCK BLU SYSTEM PLATE, 12 HOLE WIDE LADDER

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HRS·February 15, 2019

    POD PACKING COIL

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code HCG·February 4, 2020

    CORTICAL BONE SCREW, 4X26MM

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code HSB·March 4, 2022

    BD RAPID DETECTION OF SARS-COV-2 VERITOR

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code QKP·January 22, 2021