BEUDAMED
    7,498 results · 23ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 3 ×

    LIFEPAK 250 DEFIBRILLATOR/MONITOR

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    ZOLL E SERIES WITH 2010 AHA GUIDLINES SOFTWARE UPDATE

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    PADPRO MODEL 2001, 2001-S, 2001-C, 2001-EPS

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    LIFEPAK 300

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    HEARTSTART XL+DEFIBRILLATOR/MONITOR WITH END-TIDAL CARBON DIOXIDE MONITORING

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    LIFEPAK 12

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    POWERHEART AED G3 SEMI-AUTOMATIC, POWERHEART AED G3 AUTOMATIC, POWERHEART AED G3 PRO, POWERHEART AED G3 PLUS

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    FAST-PATCH

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    JUMP START, MODEL 970300

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    HEART SYNC, MODELS C-100 AND T-100

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    HEWLETT-PACKARD M2475B WITH 12-LEAD OPTION (#C90) CODEMASTER 100 CONITOR/DEFIBRILLATOR

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    FIRSTSAVE BIPHASIC MODELS 9200 AND 9210

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    Imager, Breast, Electrical Impedance

    FDA Pre-Market Approval
    FDA Class 3 ·T-SCAN 2000

    Prosthesis, Intervertebral Disc

    FDA Pre-Market Approval
    FDA Class 3 ·Simplify Cervical Artificial Disc

    System, Appendage Closure, Left Atrial

    FDA Pre-Market Approval
    FDA Class 3 ·WATCHMAN FLX Left Atrial Appendage Closure Device with Delivery System and WATCHMAN Left Atrial Appendage Closure Device

    Immunohistochemistry Assay, Antibody, Programmed Death-Ligand 1

    FDA Pre-Market Approval
    FDA Class 3 ·PD-L1 IHC 28-8 pharmDx

    Lenses, Soft Contact, Extended Wear

    FDA Pre-Market Approval
    FDA Class 3 ·O2 OPTIX (LOTRAFILCON B) AND NIGHT AND DAY (LOTRAFILCON A) SOFT CONTACT LENSES FOR EXTENDED WEAR

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·SUREFIX TM MODEL 5072 LEAD

    Coronary Drug-Eluting Stent

    FDA Pre-Market Approval
    FDA Class 3 ·ORSIRO Sirolimus Eluting Coronary Stent System

    Immunohistochemistry Assay, Antibody, Anaplastic Lymphoma Kinase

    FDA Pre-Market Approval
    FDA Class 3 ·VENTANA ALK (D5F3) CDX ASSAY