BEUDAMED
    390 results · 24ms · Sources: EU EUDAMED, US FDA

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    2520274-2013-04849

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code JDS·August 14, 2013

    MMT-712 PARADIGM INSULIN PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LZG·December 19, 2024

    MMT-712 PARADIGM INSULIN PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LZG·January 23, 2025

    MMT-712 PARADIGM INSULIN PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LZG·January 23, 2025

    ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·CORDIS NEUROVASCULAR, INC.·Product code NJE·April 26, 2011

    BEAR

    FDA Adverse Event
    Malfunction ·VIASYS RESPIRATORY CARE INC.·Product code CBK·July 17, 2006

    STARLIMS PUBLIC HEALTH SOLUTION

    FDA Adverse Event
    Malfunction ·ABBOTT INFORMATICS CORPORATION·Product code JQP·June 21, 2016

    LATEX-FREE O-RINGS 100PK

    FDA Adverse Event
    Malfunction ·INTEGRA YORK, PA INC.·Product code EXX·April 26, 2012

    ROTO-LOK HUNTER GRASPER 3.5 X 24

    FDA Adverse Event
    Malfunction ·Product code EXX·December 7, 2010

    RECTAL THERMOMETER

    FDA Adverse Event
    Injury ·IVAC·Product code EXX·June 30, 1992

    PRATT RECTAL PROBE 10 IN SHAFT 7-3/4 IN

    FDA Adverse Event
    Malfunction ·Product code EXX·October 5, 2010

    RIGID CURVE POSITIONER

    FDA Adverse Event
    Malfunction ·POWER MEDICAL INTERVENTIONS·Product code EXX·September 4, 2002

    IVAC TEMP PLUS II PROBE

    FDA Adverse Event
    Malfunction ·ALARIS MEDICAL SYSTEMS·Product code EXX·June 30, 2004

    MCGIVNEY HEMO LIGATOR 7

    FDA Adverse Event
    Malfunction ·INTEGRA, YORK - IMILTEX·Product code EXX·November 4, 2011

    HEAT PROBE

    FDA Adverse Event
    Injury ·OLYMPUS CORPORATION·Product code EXX·July 6, 1992

    UNIFIX ANORECTAL BALLOON HOLDER

    FDA Adverse Event
    Other ·SANDHILL SCIENTIFIC, INC.·Product code EXX·November 14, 2013

    MAMM MR 8G BLADELESS PROBE SET

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code EXX·August 7, 2010

    VCL+ UD 27IN 4-0 S/A SH-1

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAM·February 3, 2022

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP MMT-523LNAL

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 17, 2017

    VIPA Veronikis Intra-Fiberoptic Pelvic Assistant, Set Catalog No 350-370. VIPA Set Includes: VIPA Urethropexy Tip Catalog No. 350-374 (Also sold individually); VIPA Urethropexy Elbow Catalog No. 350-375 (also sold individually); VIPA Vaginal Cuff Tips (small) Catalog No. 350-376 (Also sold individually); VIPA Vaginal Cuff Tips (large) Catalog No. 350-378 (Also sold individually); VIPA Rectal Probe Catalog No. 350-380 (Also sold Individually); VIPA Fiber Optic Cable (Storz to ACMI Connection) Catalog No. 350-372 (Also sold individually). For use in Urethropexy Procedures and Paravaginal Repairs (accurate suture placement by illuminating the anatomy lateral to the bladder neck); in Sacrocolpopexy (steadies the vaginal vault and provides a suture platform with fiberoptic illumination); in Vaginal surgery (illuminates the rectum to visualize endometriosis lesions on the rectovaginal septum).

    FDA Recall
    Terminated ·Marina Medical Instruments Inc.·Product code EXX·April 9, 2009