BEUDAMED
    9,195 results · 55ms · Sources: EU EUDAMED, US FDA

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    FDA UDI
    SOUTHERN IMPLANTS (PTY) LTD·06009544011095·Instrument, Fibula Holder

    AQUA+I-F, I-H, I-FH, II-H, II-FH, III-H

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    READY TO WEAR DENTAL PROTECTOR

    FDA Adverse Event
    RANIR LLC·Product code OBR·October 12, 2015

    TRANSDUCER X7-2T

    FDA Adverse Event
    Malfunction ·PHILIPS ULTRASOUND INC.·Product code JOP·June 8, 2022

    SURELIFE

    FDA Adverse Event
    Malfunction ·MHC MEDICAL PRODUCTS, LLC.·Product code DXN·July 11, 2018

    SYSTEM, TEST, BLOOD GLUCOSE, OVER THE COUNTER

    FDA Adverse Event
    Malfunction ·MHC MEDICAL PRODUCTS, LLC·Product code NBW·June 6, 2018

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·August 27, 2014

    GRIND NO MORE

    FDA Adverse Event
    Injury ·RANIR, LLC·Product code OBR·October 21, 2014

    SURESCAN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·February 1, 2016

    TOTALCARE BARIATRIC

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·June 3, 2010

    NO INFORMATION

    FDA Adverse Event
    Injury ·UNKNOWN·Product code DZE·August 11, 2022

    LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code GDO·September 30, 2005

    GE

    FDA Adverse Event
    Injury ·Product code LNH·July 19, 2011

    NCP PULSE GENERATOR

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·October 26, 2001

    PERITONEAL DIALYSIS CATHETER

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code FJS·August 12, 2023

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 11, 2014

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Injury ·ROCHE DIAGNOSTICS CORP.·Product code LFR·October 26, 2007

    Medtronic KYPHON(R) Express(TM) Directional Bone Filler Device, SIZE 2, REF FB, QTY 1 EA, Rx only STERILE R

    FDA Recall
    Terminated ·Medtronic Sofamor Danek USA Inc·Product code OAR·December 6, 2017

    AMS 700 CX MS PUMP

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code JCW·January 8, 2025

    ECLIPSE TREATMENT PLANNING SYSTEM

    FDA Adverse Event
    Malfunction ·VARIAN MEDICAL SYSTEMS, INC.·Product code MUJ·July 13, 2012