BEUDAMED
    10,000 results · 68ms · Sources: EU EUDAMED, US FDA

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    Geysir CDD 1050 basic

    Device
    EU MDR · Eu Md Class 2a ·LISCHKA GmbH·On the market·12 countries

    Geysir CDD 1060 basic

    Device
    EU MDR · Eu Md Class 2a ·LISCHKA GmbH·On the market·12 countries

    Geysir CDD 1050 basic

    Device
    EU MDD · Eu Md Class 2a ·LISCHKA GmbH·On the market·12 countries

    Geysir CDD 1090 basic

    Device
    EU MDR · Eu Md Class 2a ·LISCHKA GmbH·On the market·12 countries

    AMTAI

    FDA UDI
    AMTAI MEDICAL EQUIPMENT, INC.·00811889031012·Surgical Light, 625 (cam)+725+725, 110V

    Welch Allyn, Inc.

    FDA UDI
    WELCH ALLYN, INC.·00732094268157·ELI250c 12-Lead Multi-Channel Electrocardiograp...

    CDD-PCA(TM) MODEL 5800R AMBULATORY INFUSION PUMP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    AMTAI

    FDA UDI
    AMTAI MEDICAL EQUIPMENT, INC.·00811889031074·Surgical Light, 625 (cam)+725+725, 110V, Intell...

    EVIS LUCERA ULTRASOUND GASTROVIDEOSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code ODG·June 17, 2022

    SILK SUTURE UNKNOWN PRODUCT

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

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

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

    KYPHON® HV-R® BONE CEMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·May 29, 2025

    CADD-LEGACY DUODOPA AMBULATORY INFUSION PUMP

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LZH·July 8, 2020

    FLUOROSCOPIC X-RAY

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·November 5, 2007

    CDD-SOLIS AMBULATORY INFUSION PUMP

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL·Product code MEA·April 24, 2014

    EVIS LUCERA ELITE BRONCHOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code EOQ·February 20, 2025

    UNK - DISTRACTOR IMPLANTS: CURVILINEAR

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code MQN·May 3, 2021

    EVIS EXERA III BRONCHOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code EOQ·September 19, 2024

    EVIS LUCERA GASTROINTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Death ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDS·May 4, 2021

    COLONOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDF·October 20, 2025