BEUDAMED
    17 results · 21ms · Sources: EU EUDAMED, US FDA

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    GE HealthCare ViewPoint 6, Catalog Number H47601AA; Radiological image processing system

    FDA Enforcement
    Class II ·Ongoing·GE Healthcare GmbH·December 24, 2025

    Jay M5s

    Device
    EU MDR · Eu Md Class 1 ·ellen wille THE HAIR-COMPANY GmbH·On the market·31 countries

    Jay M51s

    Device
    EU MDR · Eu Md Class 1 ·ellen wille THE HAIR-COMPANY GmbH·On the market·31 countries

    Jay M44s

    Device
    EU MDR · Eu Md Class 1 ·ellen wille THE HAIR-COMPANY GmbH·On the market·31 countries

    Jay M3s

    Device
    EU MDR · Eu Md Class 1 ·ellen wille THE HAIR-COMPANY GmbH·On the market·31 countries

    Jay M38s

    Device
    EU MDR · Eu Md Class 1 ·ellen wille THE HAIR-COMPANY GmbH·On the market·31 countries

    Jay M34s

    Device
    EU MDR · Eu Md Class 1 ·ellen wille THE HAIR-COMPANY GmbH·On the market·31 countries

    Jay M17s

    Device
    EU MDR · Eu Md Class 1 ·ellen wille THE HAIR-COMPANY GmbH·On the market·31 countries

    JAY Shape

    Device
    EU MDR · Eu Md Class 1 ·Sunrise Medical GmbH·On the market·7 countries

    Jay M56/60s

    Device
    EU MDR · Eu Md Class 1 ·ellen wille THE HAIR-COMPANY GmbH·On the market·31 countries

    Jay Back

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·Sunrise Medical GmbH·1 device

    pricon GmbH & Co.KG

    Importer
    🇩🇪 Germany·2 Manufacturers

    Macrogol TAD

    Basic UDI-DI
    EU MDD · Eu Md Class 2a ·TAD Pharma GmbH·1 device

    Dimension Vista¿ Homocysteine Flex Reagent Cartridge (HCYS), Device Listing No.: D017878 is an in vitro diagnostic test for the quantitative measurement of total homocysteine in human serum, heparinized plasma and EDTA plasma on the Dimension Vista System.

    FDA Enforcement
    Class II ·Terminated·CSL Behring GmbH·July 27, 2016

    Centrifuge 5430; Centrifuge 5430R

    Basic UDI-DI
    EU IVDR · Eu Ivd Class A ·Eppendorf SE·8 devices

    ARCHITECT DHEA-S Reagent Product Usage: It is a chemiluminescent microparticle immunoassay (CMIA) for the quantitative determination of dehydroepiandrosterone sulfate (DHEA-S) in human serum and plasma on the ARCHITECT iSystem.

    FDA Enforcement
    Class II ·Terminated·Abbott Gmbh & Co. KG·May 16, 2018

    Trusetal Verbandstoffwerk GmbH

    Importer
    🇩🇪 Germany·9 Manufacturers