Information supplied by the manufacturer of medical devices Ingestion-build-221493 Initial settings

Initial settings

Products supplied sterile

6 Procedure

This key document gives guidance for decisions during the design of machinery and will assist in the preparation of consistent and appropriate Type-B and Type-C standards in order to comply with the essential safety and health requirements

EN 50131-1

Information supplied by the manufacturer of medical devices Ingestion-build-221493 Initial settingsWhat is this standard about? It exists to help medical device manufacturers comply with the information requirements of the European medical device directives. Who is this standard for? Manufacturers of medical devices Why should you use this standard? It specifies requirements for information to be supplied by manufacturers of medical devices regulated by Council Directive 90 385 EEC relating to active implantable medical devices and Council