+Article 33 1
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Article 33 1
1. Before making an EHR system available on the market, distributors shall verify that:
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(a)
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the manufacturer has drawn up the EU declaration of conformity;
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(b)
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the EHR system bears the CE marking of conformity;
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(c)
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the EHR system is accompanied by the information sheet referred to in Article 38 with clear and complete instructions for use in accessible formats;
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(d)
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where applicable, the importer has complied with the requirements set out in Article 32(3).
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1. Pregled
1.1 Reference
1.2 Utvrđeni zahtjevi
1.3 Povezani standardi
2. Utvrđeni zahtjevi
3. Povezani standardi
- Builddate: 05.03.2025 00:00:00 -Doknr: CELEX:32025R0327
- EULAW -
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