BEUDAMED
    3,050 results · 43ms · Sources: EU EUDAMED, US FDA

    System, Nucleic Acid Amplification, Mycobacterium Tuberculosis Complex

    FDA Pre-Market Approval
    FDA Class 2 ·GEN-PROBE(R) AMPLIFIED MYCOBACTERIUM TUBERCULOSIS DIRECT TEST (MTD TEST)

    Automated External Defibrillators (Non-Wearable)

    FDA Pre-Market Approval
    FDA Class 3 ·ZOLL X Series, Propaq MD, and X Series Advanced

    Ring, Endocapsular

    FDA Pre-Market Approval
    FDA Class 3 ·CAPSULAR TENSION RING AND STABILEYES

    Automated External Defibrillators (Non-Wearable)

    FDA Pre-Market Approval
    FDA Class 3 ·LIFEPAK CR® Plus Defibrillator, LIFEPAK EXPRESS® Defibrillator, and CHARGE-PAK® Battery Charger

    Automated External Defibrillators (Non-Wearable)

    FDA Pre-Market Approval
    FDA Class 3 ·Powerheart G5 Automated External Defibrillator

    Automated External Defibrillators (Non-Wearable)

    FDA Pre-Market Approval
    FDA Class 3 ·HeartSine samaritan Public Access Automated External Defibrillators (SAM 350P, SAM 360P, and SAM 450P) and Accessories

    System, Nucleic Acid Amplification, Mycobacterium Tuberculosis Complex

    FDA Pre-Market Approval
    FDA Class 2 ·AMPLICOR (TM) MYCOBACTERIUM TUBERCULOSIS TEST

    Automated External Defibrillators (Non-Wearable)

    FDA Pre-Market Approval
    FDA Class 3 ·LIFEPAK Automated External Defibrillators

    System, Nucleic Acid Amplification, Mycobacterium Tuberculosis Complex

    FDA Pre-Market Approval
    FDA Class 2 ·GEN-PROBE(R) AMPLIFIED MYCOBACTERIUM TUBERCULOSIS DIRECT TEST (MTD TEST)

    Automated External Defibrillators (Non-Wearable)

    FDA Pre-Market Approval
    FDA Class 3 ·QUIK-COMBO® Therapy Cable

    Ring, Endocapsular

    FDA Pre-Market Approval
    FDA Class 3 ·RingJect and Capsular Tension Ring (CTR)

    Automated External Defibrillators (Non-Wearable)

    FDA Pre-Market Approval
    FDA Class 3 ·QUIK-COMBO® Therapy Cable (a necessary AED accessory of the LIFEPAK® 15 Monitor/Defibrillator)

    Automated External Defibrillators (Non-Wearable)

    FDA Pre-Market Approval
    FDA Class 3 ·X Series®, R Series®, AED Pro®, AED 3™ BLS Professional Defibrillators, Pro-Padz Radiotransparent Electrode, SurePower™

    Automated External Defibrillators (Non-Wearable)

    FDA Pre-Market Approval
    FDA Class 3 ·samaritan Public Access Automated External Defibrillators and Accessories

    Automated External Defibrillators (Non-Wearable)

    FDA Pre-Market Approval
    FDA Class 3 ·LIFEPAK® 15 monitor/defibrillator

    Automated External Defibrillators (Non-Wearable)

    FDA Pre-Market Approval
    FDA Class 3 ·Avive Automated External Defibrillator (AED) System

    Automated External Defibrillators (Non-Wearable)

    FDA Pre-Market Approval
    FDA Class 3 ·AED 3 Defibrillator with Uni-Padz

    System, Nucleic Acid Amplification, Mycobacterium Tuberculosis Complex

    FDA Pre-Market Approval
    FDA Class 2 ·GEN-PROBE(R) AMPLIFIED MYCOBACTERIUM TUBERCULOSIS DIRECT TEST (MTD TEST)

    Care bed ELBUR PB 325 MW

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·Elbur spółka z ograniczoną odpowiedzialnością spółka komandytowa·1 device

    Aucheer MW-01 Test cartridge incubator

    Basic UDI-DI
    EU IVDR · Eu Ivd Class A ·NINGBO AUCHEER BIOTECHNOLOGY CO.,LTD.·1 device