+Article 62 6.

Article 62 6.

The application shall not include the risks to human health arising from the use of a substance in a medical device regulated by Directives 90/385/EEC, 93/42/EEC or 98/79/EC.

1. Panoramica

Titolo	Regolamentazione

1.1 Riferimenti

1.2 Requisiti identificati

1.3 Standard correlati

2. Requisiti identificati

Requisiti
Fonte	Requisito

3. Standard correlati

Standard
Fonte	Requisito

Builddate: 22.06.2026 00:00:00 -Doknr: CELEX:32006R1907
EULAW -
European Regulation published on http://eur-lex.europa.eu/