Digistat Surgical Information System (SIS) is the comprehensive solution for every staff member's demands for the Surgical workflow. It eases the demanding workload of surgical procedures. From appointment scheduling to operating-room planning, from anesthesia to surgery documentation, from stockroom management to optimal use of resources, this solution brings significant benefits to the main aspects of surgical workflow and its main actors. Digistat SIS - with an intuitive and touch-screen user interface - can cut down expenditure and help to improve performance, efficiency and results. Digistat SIS is a Class I medical device in EU/EFTA according to the medical devices directives (93/42/EEG as amended).
Digistat Surgical Information System (SIS) is the comprehensive solution for every staff member's demands for the Surgical workflow. It eases the demanding workload of surgical procedures. From appointment scheduling to operating-room planning, from anesthesia to surgery documentation, from stockroom management to optimal use of resources, this solution brings significant benefits to the main aspects of surgical workflow and its main actors. Digistat SIS - with an intuitive and touch-screen user interface - can cut down expenditure and help to improve performance, efficiency and results. Digistat SIS is a Class I medical device in EU/EFTA according to the medical devices directives (93/42/EEG as amended).
Digistat Surgical Information System (SIS) is the comprehensive solution for every staff member's demands for the Surgical workflow. It eases the demanding workload of surgical procedures. From appointment scheduling to operating-room planning, from anesthesia to surgery documentation, from stockroom management to optimal use of resources, this solution brings significant benefits to the main aspects of surgical workflow and its main actors. Digistat SIS - with an intuitive and touch-screen user interface - can cut down expenditure and help to improve performance, efficiency and results. Digistat SIS is a Class I medical device in EU/EFTA according to the medical devices directives (93/42/EEG as amended).
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