BEUDAMED
    4,690 results · 20ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 3 ×

    Implanted Phrenic Nerve Stimulator For Central Sleep Apnea

    FDA Pre-Market Approval
    FDA Class 3 ·Remede® System

    Implanted Phrenic Nerve Stimulator For Central Sleep Apnea

    FDA Pre-Market Approval
    FDA Class 3 ·remede® System

    Implanted Phrenic Nerve Stimulator For Central Sleep Apnea

    FDA Pre-Market Approval
    FDA Class 3 ·remede® System

    Sensor, Glucose, Invasive

    FDA Pre-Market Approval
    FDA Class 3 ·GST (MINILINK TRANSMITTER) & GSR (CGMS I PRO RECORDER)

    Filler, Bone Void, Non-Osteoinduction

    FDA Pre-Market Approval
    FDA Class 3 ·NORIAN SKELETAL REPAIR SYSTEM (SRS) CANCELLOUS BONE CEMENT

    Paste, Injectable For Vocal Cord Augmentation

    FDA Pre-Market Approval
    FDA Class 3 ·MENTOR POLYTEF PASTE /FOR INJECTION

    Paste, Injectable For Vocal Cord Augmentation

    FDA Pre-Market Approval
    FDA Class 3 ·POLYTEF PASTE FOR INJECTION

    Paste, Injectable For Vocal Cord Augmentation

    FDA Pre-Market Approval
    FDA Class 3 ·MENTOR POLYTEF PASTE FOR INJECTION

    Paste, Injectable For Vocal Cord Augmentation

    FDA Pre-Market Approval
    FDA Class 3 ·MENTOR POLYTEF PASTE FOR INJECTION

    Paste, Injectable For Vocal Cord Augmentation

    FDA Pre-Market Approval
    FDA Class 3 ·MENTOR POLYTEF PASTE FOR INJECTION

    Paste, Injectable For Vocal Cord Augmentation

    FDA Pre-Market Approval
    FDA Class 3 ·POLYTEF PASTE FOR VOCAL CORD INJECTION

    Transurethral Occlusion Insert, Urinary Incontinence-Control, Female

    FDA Pre-Market Approval
    FDA Class 3 ·RELIANCE URINARY CONTROL INSERT & SIZING DEVICE

    Transurethral Occlusion Insert, Urinary Incontinence-Control, Female

    FDA Pre-Market Approval
    FDA Class 3 ·RELIANCE URINARY CONTROL INSERT AND SIZING DEVICE

    Aid, Surgical, Viscoelastic

    FDA Pre-Market Approval
    FDA Class 3 ·VITRAX SODIUM HYALURONATE

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL AC-21 OMNIFIT ANTERIOR CHAMBER

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 304 (ULTRA C-LOOP)

    Next Generation Sequencing Oncology Panel, Somatic Or Germline Variant Detection System

    FDA Pre-Market Approval
    FDA Class 3 ·FoundationOne CDx (F1CDx)

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·CM(TM) LENSES

    Next Generation Sequencing Oncology Panel, Somatic Or Germline Variant Detection System

    FDA Pre-Market Approval
    FDA Class 3 ·FoundationOne CDx

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 304 (ULTRA C-LOOP)