BEUDAMED
    7,312 results · 51ms · Sources: EU EUDAMED, US FDA

    Assay, Oral Direct Thrombin Inhibitor

    FDA classification
    FDA Not Classified ·Assay, Oral Direct Thrombin Inhibitor

    MED 31220

    Certificate
    MDD Annex II (excluding section 4)·DBM SRL·KIWA CERMET ITALIA S.P.A.·3 Basic UDI-DIs

    DD60149886

    Certificate
    MDD Annex V·Dam S.r.l.·TUV Rheinland Italia SRL·1 Basic UDI-DI

    CO2 D.M. COLTURA CELLULARE Pacco 12x40 Litri Valv. REGULAR

    Basic UDI-DI
    EU MDD · Eu Md Class 2a ·Air Liquide Sanità Service S.p.A.·1 device

    CO2 D.M. COLTURA CELLULARE Bombola 5 Litri Valv. REGULAR

    Basic UDI-DI
    EU MDD · Eu Md Class 2a ·Air Liquide Sanità Service S.p.A.·1 device

    CO2 D.M. COLTURA CELLULARE Bombola 40 Litri Valv. REGULAR

    Basic UDI-DI
    EU MDD · Eu Md Class 2a ·Air Liquide Sanità Service S.p.A.·1 device

    CO2 D.M. COLTURA CELLULARE Bombola 14 Litri Valv. REGULAR

    Basic UDI-DI
    EU MDD · Eu Md Class 2a ·Air Liquide Sanità Service S.p.A.·1 device

    CO2 D.M. COLTURA CELLULARE Bombola 10 Litri Valv. REGULAR

    Basic UDI-DI
    EU MDD · Eu Md Class 2a ·Air Liquide Sanità Service S.p.A.·1 device

    Dam, Rubber

    FDA classification
    FDA Class 1 ·Dam, Rubber

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·CAPSURE(R) AND CAPSURE(R)SP LEADS

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·CAPSURE(R) AND CAPSURE(R) SP PACING LEADS

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·CARBON TIPPED LEAD MODELS 1085S,1085M,& 1085K

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·SWEET TIP RX STEROID ELUTING LEAD

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·FLEXTEND BIPOLAR, STEROID ELUTING, EXTENDABLE/ RETRACTABLE PACING LEAD

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·THINLINE/FINELINE

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·SUREFIX TM MODEL 5072 LEAD

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·PASSIVE PLUS DX ENDOCARDIAL, STEROID ELUTING, PASSIVE FIXATION PACING LEADS

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·PHILOS FAMILY OF PULSE GENERATORS

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·ENDOCARDIAL PACEMAKER LEAD W/CARBON TIP

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·CARBON TIPPED LEAD ALT.PROD.TRAYS