BEUDAMED
    2,449 results · 37ms · Sources: EU EUDAMED, US FDA

    Garrett Leight California Optical

    FDA registration
    GARRETT LEIGHT EUROPE B.V.·1 product·🇳🇱 Netherlands

    Mr. Leight

    FDA registration
    GARRETT LEIGHT EUROPE B.V.·1 product·🇳🇱 Netherlands

    E-LINK Exercise System, X4, E4000, FP3 ForcePlate, M600 Exercise Kit, M800 Exercise Kit, Myo-Ex, AngleX, DG1, WK0, WK1

    FDA registration
    BIOMETRICS LTD.·1 product·🇬🇧 United Kingdom

    SCOTT'S INFUSOR TIPS 100/bg w/ BRUSH-PADDED END

    FDA UDI
    SCOTT'S DENTAL SUPPLY L.L.C.·D77819911251·SCOTT'S INFUSOR TIPS 100/bg w/ BRUSH-PADDED END

    NON-PRESCRIPTION SUNGLASSES

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    GENE-TRAK CAMPYLOBACTER ASSAY

    FDA 510(k)
    FDA Class 1 ·Microbiology

    SYNTHES HEMOSTATIC BONE PUTTY (HBP)

    FDA 510(k)
    FDA Unclassified ·Unknown

    NORIAN DRILLABLE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CURITY(R) PERCUTANEOUS CATHETERS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NORIAN REINFORCED, NORIAN REINFORCED FAST SET PUTTY

    FDA 510(k)
    FDA Class 2 ·Neurology

    ORTHOMESH

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SYNTHES HEMOSTATIC BONE PUTTY

    FDA 510(k)
    FDA Unclassified ·Unknown

    DG 3 D N.1 V=100 STÜ Superior CE

    Device
    EU IVDR · Eu Ivd Class A ·Paul Marienfeld GmbH & Co. KG·On the market·32 countries

    DG 3 D N.0 V=100 STÜ Superior CE

    Device
    EU IVDR · Eu Ivd Class A ·Paul Marienfeld GmbH & Co. KG·On the market·32 countries

    DG 3 D N.3 V=50 STÜ Superior CE

    Device
    EU IVDR · Eu Ivd Class A ·Paul Marienfeld GmbH & Co. KG·On the market·32 countries

    Device, Removal, Pacemaker Electrode, Percutaneous

    FDA Pre-Market Approval
    FDA Class 3 ·SPECTRANETICS LASER SHEATH (SLS) CATHETERS

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·SECURA DR/VR/MAXIMO II VR/DR/VIRTUOSO II DR/VR ICDS

    Pulse-Generator, Single Chamber, Sensor Driven, Implantable

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 2090 MEDTRONIC CARELINK PROGRAMMER

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·JEWEL AF/GEM III AT/CS-SVC TRANSVENE LEAD

    Implantable Pacemaker Pulse-Generator

    FDA Pre-Market Approval
    FDA Class 3 ·MEDA-MV PACING SYSTEM