BEUDAMED
    2,630 results · 38ms · Sources: EU EUDAMED, US FDA

    System, Test, Her-2/Neu, Nucleic Acid Or Serum

    FDA Pre-Market Approval
    FDA Class 3 ·ONCOR(R) AMPLITECT(TM) HER/NEU(ERBB2)GENE AMPLIFI

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VITALITY AUTOMATIC IMPLANTABLE CARDIOVERTER DEFIBRILLATOR (AICD) SYSTEMS

    Spinal Pedicle Screw, Fixation, Appliance System

    FDA Pre-Market Approval
    FDA Class 3 ·SABER LUMBAR I/F CAGE, JAGUAR LUMBAR I/F CAGE

    Ferricyanide, Glucose

    FDA classification
    FDA Class 2 ·Ferricyanide, Glucose

    Igg, Ferritin, Antigen, Antiserum, Control

    FDA classification
    FDA Class 2 ·Igg, Ferritin, Antigen, Antiserum, Control

    Stimulator, Autonomic Nerve, Implanted (Depression)

    FDA classification
    FDA Class 3 ·Stimulator, Autonomic Nerve, Implanted (Depression)

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·VISTA LORDOTIC INTERBODY FUSION CAGE

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VITALITY AVT AND THE PROGRAMMER SOFTWARE APPLICATION MODEL 2812

    Filler, Recombinant Human Bone Morphogenetic Protein, Collagen Scaffold With Metal Prosthesis, Osteoinduction

    FDA Pre-Market Approval
    FDA Class 3 ·INFUSE BONE GRAFT/LT-CAGE LUMBAR TAPERED FUSION DEVICE

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK INTERBODY FUSION SYSTEM, BP/LORDOTIC DEVICE

    Separator, Automated, Blood Cell And Plasma, Therapeutic

    FDA Pre-Market Approval
    FDA Unclassified ·PROSORBA COLUMN

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VENTAK VITALITY AVT AICD, MODELS A135 AND A155, MODEL 2920 PROGRAMMER WITH MODEL 2812 APPLICATION SOFTWARE VERSION 1.2

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·LT-CAGE LUMBAR TAPERED FUSION DEVICE

    Filler, Bone Void, Synthetic Peptide

    FDA Pre-Market Approval
    FDA Class 3 ·PearlMatrix™ Bone Graft

    MED-RAS GmbH Regulatory Affairs Service

    Authorized representative
    🇩🇪 Germany·18 Manufacturers·235 Devices

    Test, Volatile Organic Compounds Breath Analysis

    FDA classification
    Test, Volatile Organic Compounds Breath Analysis

    Dvd, Bluray, Or Hd Recorder

    FDA classification
    FDA Not Classified ·Dvd, Bluray, Or Hd Recorder

    HD 60144656

    Certificate
    MDD Annex II (excluding section 4)·Substrate HD·TÜV Rheinland LGA Products GmbH·1 Basic UDI-DI

    Acute Coronary Syndrome Event Detector

    FDA Pre-Market Approval
    FDA Class 3 ·Guardian System

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·LT-CAGE TAPERED FUSION DEVICE