BEUDAMED
    7,061 results · 42ms · 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.

    RAPIDPoint® 500e Blood Gas System

    FDA registration
    SIEMENS HEALTHCARE DIAGNOSTICS MANUFACTURING LTD·9 products·🇬🇧 United Kingdom

    OPTI CCA-TS2

    FDA registration
    OPTI MEDICAL SYSTEMS INC.·10 products·🇺🇸 United States

    RAPIDPoint® 500e Blood Gas System

    FDA registration
    Siemens Healthcare Diagnostics Inc·9 products·🇺🇸 United States

    MICRO ELECTRODE CA++

    FDA registration
    ROCHE DIAGNOSTICS GMBH·12 products·🇩🇪 Germany

    RAPIDPoint® 500e Blood Gas System

    FDA registration
    Siemens Healthcare Diagnostics Inc.·9 products·🇺🇸 United States

    Novamedisan Italia Srl

    Importer
    🇮🇹 Italy·5 Manufacturers

    SARS-CoV-2 and Influenza A/B Virus Multiplex Nucleic Acid Diagnostic Kit (PCR-Fluorescence Probing)

    Device
    EU IVDD · Eu Ivd General ·Sansure Biotech Inc.·On the market

    SARS-CoV-2 and Influenza A/B Virus Multiplex Nucleic Acid Diagnostic Kit (PCR-Fluorescence Probing)

    Device
    EU IVDD · Eu Ivd General ·Sansure Biotech Inc.·On the market

    Novel Coronavirus (SARS-CoV-2)/Respiratory Pathogens Multiplex Panel Nucleic Acid Diagnostic Kit (PCR-Fluorescence Probing)

    Device
    EU IVDD · Eu Ivd General ·Sansure Biotech Inc.·On the market

    Novel Coronavirus (SARS-CoV-2)/Respiratory Pathogens Multiplex Panel Nucleic Acid Diagnostic Kit (PCR-Fluorescence Probing)

    Device
    EU IVDD · Eu Ivd General ·Sansure Biotech Inc.·On the market

    Freeze-dried SARS-CoV-2/Influenza A/Influenza B Nucleic Acid Combined Detection Kit (Fluorescence PCR)

    Device
    EU IVDD · Eu Ivd General ·Jiangsu Macro & Micro-Test Med-Tech Co., Ltd.·On the market

    SARS-COV-2 Nucleocapsid (N) Antigen Rapid Detection Kit (Colloidal gold method) Saliva Test lollopop style

    Device
    EU IVDD · Eu Ivd General ·Nanjing Synthgene Medical Technology Co., Ltd. ·On the market

    Sars-Cov-2 Serology Test

    FDA classification
    FDA Class 2 ·Sars-Cov-2 Serology Test

    Test, Prostate Specific Antigen, Free, (Noncomplexed) To Distinguish Prostate Cancer From Benign Conditions

    FDA Pre-Market Approval
    FDA Class 3 ·DIMENSION FPSA FLEX REAGENT CARTRIDGE

    Test, Prostate Specific Antigen, Free, (Noncomplexed) To Distinguish Prostate Cancer From Benign Conditions

    FDA Pre-Market Approval
    FDA Class 3 ·Dimension Vista FPSA Flex reagent cartridge (K6452)

    Test, Prostate Specific Antigen, Free, (Noncomplexed) To Distinguish Prostate Cancer From Benign Conditions

    FDA Pre-Market Approval
    FDA Class 3 ·Dimension FPSA Flex Reagent Cartridge

    Test, Prostate Specific Antigen, Free, (Noncomplexed) To Distinguish Prostate Cancer From Benign Conditions

    FDA Pre-Market Approval
    FDA Class 3 ·DIMENSION FPSA FLEX REAGENT CARTRIDGE AND DIMENSION VISTA FPSA FLEX REAGENT CARTRIDGE

    Test, Prostate Specific Antigen, Free, (Noncomplexed) To Distinguish Prostate Cancer From Benign Conditions

    FDA Pre-Market Approval
    FDA Class 3 ·DIMENSION FPSA FLEX REAGENT CARTRIDGE

    Test, Prostate Specific Antigen, Free, (Noncomplexed) To Distinguish Prostate Cancer From Benign Conditions

    FDA Pre-Market Approval
    FDA Class 3 ·Dimension FPSA Flex reagent cartridge (RF451)

    Test, Prostate Specific Antigen, Free, (Noncomplexed) To Distinguish Prostate Cancer From Benign Conditions

    FDA Pre-Market Approval
    FDA Class 3 ·DIMENSION FPSA FLEX REAGENT CARTRIDGE