BEUDAMED
    11 results · 8ms · Sources: EU EUDAMED, US FDA

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    Filters Notified Body: Intertek Semko Ab ×

    41319433-05

    Certificate
    MDD Annex II (excluding section 4)·Cynosure LLC·INTERTEK SEMKO AB·342 Basic UDI-DIs

    41313861

    Certificate
    MDD Annex II (excluding section 4)·Diagnosys LLC·INTERTEK SEMKO AB·11 Basic UDI-DIs

    41319433-05

    Certificate
    MDD Annex II (excluding section 4)·Cynosure LLC·INTERTEK SEMKO AB·18 Basic UDI-DIs

    41343861

    Certificate
    MDD Annex II Section 4·Diagnosys LLC·INTERTEK SEMKO AB·1 Basic UDI-DI

    41371240

    Certificate
    MDD Annex II (excluding section 4)·X-Nav Technologies, LLC·INTERTEK SEMKO AB·4 Basic UDI-DIs

    41371240-03

    Certificate
    MDD Annex II (excluding section 4)·X-Nav Technologies, LLC·INTERTEK SEMKO AB·12 Basic UDI-DIs

    41377776-04

    Certificate
    MDD Annex II (excluding section 4)·Spectra Medical Devices, LLC·INTERTEK SEMKO AB·4 Basic UDI-DIs

    41377748-01

    Certificate
    MDD Annex II (excluding section 4)·American Surgical Company, LLC·INTERTEK SEMKO AB·1 Basic UDI-DI

    41377747-01

    Certificate
    MDD Annex II Section 4·American Surgical Company, LLC·INTERTEK SEMKO AB·2 Basic UDI-DIs

    413106295

    Certificate
    MDD Annex II (excluding section 4)·Pressure Products Medical Device Manufacturing LLC.·INTERTEK SEMKO AB·1 Basic UDI-DI

    413106296

    Certificate
    MDD Annex II Section 4·Pressure Products Medical Device Manufacturing LLC.·INTERTEK SEMKO AB·1 Basic UDI-DI