BEUDAMED
    1,651 results · 67ms · Sources: EU EUDAMED, US FDA

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    FIELDER 18

    FDA Adverse Event
    Injury ·ASAHI INTECC CO., LTD.·Product code OCY·June 24, 2024

    APEX HP M ADULST HOLLOW FIBER MEMBRANE OXYGENATOR

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·March 13, 2013

    Clearview hCG Combo with Reference Line, Wampole Laboratories, ABI List No/Product No. 6028KCV; 30 Individually pouched test cassettes with disposable pipettes, 1 Directional Insert; Inverness Medical Professional Diagnostics Group; Marketed by Wampole Laboratories, 2 Research Way, Princeton NJ 08540 USA

    FDA Recall
    Terminated ·Applied Biotech Inc·Product code JHI·September 28, 2006

    INSPIRE 8F: HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER AND HARDSHEL

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·March 15, 2019

    EVIS LUCERA ELITE GASTROINTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code FDS·May 24, 2024

    SINGLE USE ELECTROSURGICAL KNIFE KD-650

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code KNS·November 21, 2023

    EKOSONIC ENDOVASCULAR CATHETER

    FDA Adverse Event
    Injury ·EKOS CORPORATION·Product code KRA·September 11, 2018

    Clearview hCG Combo Waived for urine & Moderate for serum, Wampole Laboratories, ABI List No/Product No. 6026KCV; Contents 30 Individually pouched test cassettes with disposable pipettes, 1 Directional Insert; Inverness Medical Professional Diagnostics Group; Marketed by Wampole Laboratories, 2 Research Way, Princeton NJ 08540 USA

    FDA Recall
    Terminated ·Applied Biotech Inc·Product code JHI·September 28, 2006

    SINGLE USE ELECTROSURGICAL KNIFE

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code KNS·July 26, 2024

    DISPOSABLE DISTAL ATTACHMENT

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code FDS·July 26, 2024

    CLIP

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code PKL·July 26, 2024

    EVIS LUCERA GASTROINTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code FDS·July 26, 2024

    EVIS LUCERA DUODENOVIDEOSCOPE

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code FDT·August 7, 2023

    UNKNOWN GII ANCHOR

    FDA Adverse Event
    Injury ·DEPUY MITEK LLC US·Product code JDR·November 4, 2019

    EVIS LUCERA DUODENOVIDEOSCOPE

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code FDT·February 6, 2024

    UNKNOWN BIO-INTRAFIX

    FDA Adverse Event
    Injury ·DEPUY MITEK LLC US·Product code HWC·October 8, 2019

    URETERO-RENO FIBERSCOPE

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code FGB·October 6, 2023

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWC·January 25, 2019

    PLATE FIXATION, BONE

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HRS·January 25, 2019

    PLATE FIXATION, BONE

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HRS·January 25, 2019