BEUDAMED
    FDA Registration Active 🇩🇪 Germany

    Pulsion Pulsiocath

    Reg #: 3003263092 · FEI: 3003263092 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    3
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    PULSION MEDICAL SYSTEMS SE
    Registration Number
    3003263092
    FEI Number
    3003263092
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Hans-Riedl-Strasse 17
    City
    Feldkirchen Bavaria
    Country
    DE

    Regulatory Submissions

    510(k) Number
    K991886

    Owner / Operator

    Firm Name
    Maquet Critical Care AB
    Operator Number
    9036213
    Address
    ROENTGENVAGEN 2
    City
    Solna
    State
    SE-NOTA
    Postal Code
    SE-17154
    Country
    SE

    Products

    Device Name Product Code
    Probe, Thermodilution KRB

    Proprietary Names

    Pulsion Pulsiocath Pulsion PCCO Monitoring Kit (PV8103, PV8115, PV8115CVP) Pulsion Pulsiocath, PiCCO Monitorin

    Establishment Types

    Manufacture Medical Device