Information supplied by the manufacturer of medical devices Ingestion-build-221493 This European Standard supersedes BS

This European Standard supersedes BS 2011-1

The scope includes pipes (collectively referred to as “jacking pipes”) intended to be installed by pipe jacking

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

Information supplied by the manufacturer of medical devices Ingestion-build-221493 This European Standard supersedes BSWhat 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