+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. Resumen

Título	Regulación

1.1 Referencias

1.2 Requisitos identificados

1.3 Estándares relacionados

2. Requisitos identificados

Requisitos
Fuente	Requisito

3. Estándares relacionados

Estándares
Fuente	Requisito

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