BEUDAMED
    6,067 results · 38ms · Sources: EU EUDAMED, US FDA

    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

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK VISTA INTERBODY FUSION DEVICE

    HFK-3350, HFK-3352-2, HFK-3352-3, HFK-3352A, HFK-3353, HFK-3355-1, HFK-3356, HFK-3357, HFK-3358, HFK-3360, HFK-3361,

    FDA registration
    FOSHAN HUAFUKANG MEDICAL TECHNOLOGY CO. LTD·1 product·🇨🇳 China

    Assay, Enzyme Linked Immunosorbent, Hepatitis C Virus

    FDA Pre-Market Approval
    FDA Class 2 ·HOME ACCESS HEPATITIS C CHECK

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·LORDOTEC(TM) TAPERED FUSION DEVICE

    Intervertebral Fusion Device With Bone Graft, Lumbar

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

    Pulse Generator, Permanent, Implantable

    FDA Pre-Market Approval
    FDA Class 3 ·ADVISA SR MRI

    Dorsal Root Ganglion Stimulator For Pain Relief

    FDA Pre-Market Approval
    FDA Class 3 ·Axium Neurostimulator System

    Dvd, Dvd-Rom, Bluray, Hd Player

    FDA classification
    FDA Not Classified ·Dvd, Dvd-Rom, Bluray, Hd Player

    Acute Coronary Syndrome Event Detector

    FDA Pre-Market Approval
    FDA Class 3 ·AngelMed Guardian System

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VITALITY DS ICD SYSTEMS

    PREPOPlus®

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·ORTHOPLUS·45 devices

    Prostrate Cancer Genes Nucleic Acid Amplification Test System

    FDA Pre-Market Approval
    FDA Class 3 ·PROGENSA PCA3 ASSAY

    Catheter, Coronary, Atherectomy

    FDA Pre-Market Approval
    FDA Class 3 ·ROTABLATOR ROTALINK PLUS ROTATIONAL ANGIOPLASTY SYSTEM

    Intervertebral Fusion Device With Bone Graft, Lumbar

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

    Implantable Pacemaker Pulse-Generator

    FDA Pre-Market Approval
    FDA Class 3 ·ACTROS SLR+,KAIROS SL PULSE GENERATORS;SL 60-11,13,15 BP SINGLE PASS PACING LEAD;SWM 1000 B-G01.0.U

    Prosthesis, Intervertebral Disc

    FDA Pre-Market Approval
    FDA Class 3 ·PRESTIGE LP(TM) CERVICAL DISC

    Programmer, Pacemaker

    FDA Pre-Market Approval
    FDA Class 3 ·VERITY ADX XL VDR MODEL 5456I PULSE GENERATOR

    Implantable Pacemaker Pulse-Generator

    FDA Pre-Market Approval
    FDA Class 3 ·VERITY ADX XL VDR MODEL 5456I PULSE GENERATOR