It Services: Consulting, Software Development, Internet And Support Symptom Checker // Participation Competition. -The Sc Must Have A Valid Ce Marking. The Sc Must Currently Have At Least One Medical Device In The Sense Of Class I According To Directive 93/42/Eec (= Medical Devices Directive - Mdd) Or In Accordance With Class I According To Annex Viii Of Directive (Eu) 2017/745 On Medical Devices (= Medical Device Regulation / Mdr). The Tk Also Requires That The Sc Offered By The Contractor Will Be Certified As A Class Iia Mdr Medical Device In The Future. It Is Therefore Necessary That Certification For Class Iia Mdr Has At Least Been Initiated By The Responsible Body. -Quantities: 28,500 Sessions Were Completed In 2023. The Tk Assumes That At Least 30,000 Completed Sessions Will Be Achieved In The First Year After The Going Live Date, An Increase Of 30% In The 2Nd And 3Rd Years Of Use And An Increase Of Another 50% In The 4Th Year Of Use. -Duration: 12/01/204 To 11/30/2028 Details Can Be Found In The Participation Documents
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