Information supplied by the manufacturer with medical devicesThis European Standard specifies requirements for the information to be supplied by a manufacturer for different categories of medical devices, as required by the relevant EU Directives. It does not specify the language to be used for such information. It is intended to complement the specific requirements of the EU Directives on medical devices in the context of specifying means by which certain requirements can be met. If these means are followed by

Annex A (informative) Examples of legal and regulatory compliance

the flexible use of DD 8788-2 to support the development of both simple and complex learner information packages

BS ISO 22554:2007 specifies the construction

ships’ hoists

It is applicable to transmission pipelines for gases

γ-HCH (γ-BHC or lindane)

Annex A (informative) Example Information Security Event and Incident Report Forms

hot rolled products of non-alloy structural steels for general use

Manufacturer's declaration for type test

There are two alternative image interchange formats for biometric authentication systems that utilize iris recognition

and the International Labour Organization’s ILO-OSH 2001- Guidelines on occupational safety and health management systems

Examples of typical threats