BEUDAMED
    25 results · 20ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Country: Germany ×

    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

    Gründler GmbH

    Manufacturer
    🇩🇪 Germany·2 Basic UDI-DIs·2 Devices·SGS FIMKO OY

    Fiagon GmbH

    Manufacturer
    🇩🇪 Germany·14 Basic UDI-DIs·33 Devices·SGS FIMKO OY

    PAUSCH Medical GmbH

    Manufacturer
    🇩🇪 Germany·SGS FIMKO OY

    Rhyk Technologies GmbH

    Manufacturer
    🇩🇪 Germany·SGS FIMKO OY

    Jay Back

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

    RAY EUROPE GmbH

    Importer
    🇩🇪 Germany·1 Manufacturer

    pricon GmbH & Co.KG

    Importer
    🇩🇪 Germany·2 Manufacturers

    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

    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

    FI24/00000064

    Certificate
    MDR QMS·Fiagon GmbH·SGS FIMKO OY