BEUDAMED
    8,327 results · 49ms · Sources: EU EUDAMED, US FDA

    Parsortix PC1 Device

    FDA 510(k)
    FDA Class 2 ·Immunology

    GenetiSure Dx Postnatal Assay

    FDA 510(k)
    FDA Class 2 ·Immunology

    xTAG Cystic Fibrosis 39 Kit v2

    FDA 510(k)
    FDA Class 2 ·Immunology

    Implantable Pacemaker Pulse-Generator

    FDA Pre-Market Approval
    FDA Class 3 ·META MV MODEL 1202 CARDIAC PACING SYSTEM

    Implantable Pacemaker Pulse-Generator

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 1256D META MV CARDIAC PULSE GENERATOR

    Implantable Pacemaker Pulse-Generator

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 1256D META MV CARDIAC PULSE GENERATOR

    Implantable Pacemaker Pulse-Generator

    FDA Pre-Market Approval
    FDA Class 3 ·META MV MODEL 1202 CARDIAC PACING SYSTEM

    Implantable Pacemaker Pulse-Generator

    FDA Pre-Market Approval
    FDA Class 3 ·META MV MODEL 1202 CARDIAC PACING SYSTEM

    Implantable Pacemaker Pulse-Generator

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 1256D META MV CARDIAC PULSE GENERATOR

    Implantable Pacemaker Pulse-Generator

    FDA Pre-Market Approval
    FDA Class 3 ·META MV MODEL 1202 CARDIAC PACING SYSTEM

    Implantable Pacemaker Pulse-Generator

    FDA Pre-Market Approval
    FDA Class 3 ·META MV MODEL 1202 CARDIAC PACING SYSTEM

    Aid, Surgical, Viscoelastic

    FDA Pre-Market Approval
    FDA Class 3 ·HEALON,HEALON GV, & HEALON5 SODIUM HYALURONATE VISCOELASTIC

    Implantable Pacemaker Pulse-Generator

    FDA Pre-Market Approval
    FDA Class 3 ·META MV MODEL 1202 & 1202 PULSE GENERATORS

    Marburg Virus (MBV) Real Time RT-PCR Kit

    Basic UDI-DI
    EU IVDD · Eu Ivd General ·SHANGHAI ZJ BIO-TECH CO., LTD·1 device

    S613 Luna Victory

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·Pride Mobility Products Corporation·1 device

    Victory ZT

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·Pride Mobility Products Corporation·1 device

    Quantum 4Front 2

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·Pride Mobility Products Corporation·1 device

    Aid, Surgical, Viscoelastic

    FDA Pre-Market Approval
    FDA Class 3 ·Sodium Hyaluronate Ophthalmic Viscoelastic Device (OVD), Healon GV PRO

    E1 SERIES A PATELLAE, STANDARD 3-PEG, E1 SERIES A PATELLAE, THIN 3-PEG, E1 SERIES PATELLAE, ASYMMETRICAL, 3-PEG

    FDA registration
    BIOMET, INC.·4 products·🇺🇸 United States

    VANGUARD XP KNEE SYSTEM

    FDA registration
    Zimmer Biomet Canada DFE·4 products·🇨🇦 Canada