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Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC (Text with EEA relevance. )

article  100

CELEX:  02017R0745-20250110

Electronic system on market surveillance
1. The Commission, in collaboration with the Member States, shall set up and manage an electronic system to collate and process the following information:
(a) summaries of the results of the surveillance activities referred to in Article 93(4);
(b) the final inspection report referred to in Article 93(7);
(c) information in relation to devices presenting an unacceptable risk to health and safety as referred to in Article 95(2), (4) and (6);
(d) information in relation to non-compliance of products as referred to in Article 97(2);
(e) information in relation to the preventive health protection measures referred to in Article 98(2);
(f) summaries of the results of the reviews and assessments of the market surveillance activities of the Member States referred to in 93(8).
2. The information referred to in paragraph 1 of this Article shall be immediately transmitted through the electronic system to all competent authorities concerned and, where applicable, to the notified body that issued a certificate in accordance with Article 56 for the device concerned and be accessible to the Member States and to the Commission.
Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC (Text with EEA relevance. )

article  100

CELEX:  02017R0745-20250110

3. Information exchanged between Member States shall not be made public where to do so might impair market surveillance activities and co-operation between Member States.