BEUDAMED
    4,963 results · 42ms · Sources: EU EUDAMED, US FDA

    ZENITH LUXACORE AUTOMIX CORE MATERIAL (MULTIPLE)

    FDA 510(k)
    FDA Class 2 ·Dental

    ULTRA SPHERICAL AMALGAM ALLOY

    FDA 510(k)
    FDA Class 2 ·Dental

    IONOSIT SEAL

    FDA 510(k)
    FDA Class 2 ·Dental

    LIGHT CURE FILLING MATERIAL

    FDA 510(k)
    FDA Class 2 ·Dental

    Pump, Infusion, Implanted, Programmable

    FDA Pre-Market Approval
    FDA Class 3 ·ASCENDA INTRATHECAL CATHETER WITH 86 CM SPINAL SEGMENT, 66CM SPINAL SEGMENT, 86 CM SPINAL SEGMENT REVISION KIT, ACCESSOR

    GWM-01A; GWM-01B; GWM-01C; nebulizer; sshine

    FDA registration
    SINOSHINE HEALTH TECHNOLOGY CO., LTD·1 product·🇻🇳 Vietnam

    HB189NC-124; HB189NC-1733, HB189NC-1-5060; HB189NC-1-6284

    FDA registration
    SINOSHINE HEALTH TECHNOLOGY CO., LTD·1 product·🇻🇳 Vietnam

    ClinRep® Complete Kit for CDT (Carbohydrate-deficient Transferrin) in Serum

    Device
    EU IVDR · Eu Ivd Class B ·RECIPE Chemicals + Instruments GmbH·On the market·32 countries

    Defibrillator, Implantable, Dual-Chamber

    FDA Pre-Market Approval
    FDA Class 3 ·KRONOS LV-T CRT-D & LUMAX VR/DR/HF (-T) ICDS & CDT-DS

    Prosthesis, Ankle, Uncemented, Non-Constrained

    FDA Pre-Market Approval
    FDA Class 3 ·Hintermann Series H3 Total Ankle Replacement System

    Prosthesis, Ankle, Uncemented, Non-Constrained

    FDA Pre-Market Approval
    FDA Class 3 ·Hintermann Series H3 Total Ankle Replacement System

    Prosthesis, Ankle, Uncemented, Non-Constrained

    FDA Pre-Market Approval
    FDA Class 3 ·Hintermann Series H3 Total Ankle Replacement System

    Prosthesis, Ankle, Uncemented, Non-Constrained

    FDA Pre-Market Approval
    FDA Class 3 ·Hintermann Series H3 Total Ankle Replacement System

    Prosthesis, Ankle, Uncemented, Non-Constrained

    FDA Pre-Market Approval
    FDA Class 3 ·Hintermann Series H3 Total Ankle Replacement System

    Prosthesis, Ankle, Uncemented, Non-Constrained

    FDA Pre-Market Approval
    FDA Class 3 ·Hintermann Series H3 Total Ankle Replacement System

    Sekisui Diagnostics P.E.I. Inc.

    FDA registration
    Sekisui Diagnostics P.E.I. Inc.·3 products·🇨🇦 Canada

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·TVL(TM) LEAD SYSTEM

    MasimoSET® LNOP® Adt SpO2 Adult Pulse Oximeter Adhesive Sensor

    FDA UDI
    MASIMO CORPORATION·10843997000007·SpO2 Adult Pulse Oximeter Adhesive Sensor

    K1025-01-EDT

    Basic UDI-DI
    EU MDR · Eu Md Class 2a ·6 devices

    Construction Tape CDT

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·Eurotape B.V.·9 devices