Implants for surgery. Active implantable medical devices - General requirements for safety, marking and for information to be provided by the manufacturer1 Scope This part of ISO 14708 specifies requirements that are generally applicable to active implantable medical devices. NOTE 1 For particular types of active implantable medical devices, these general requirements are supplemented or modified by the requirements of particular parts of ISO 14708. The tests that are specified in ISO 14708 are type tests and are to be carried out on samples of an active implantable medical device to show compliance.

A traceability system for sustainably produced cocoa is a technical tool to assist a cocoa supply chain actor operating within a cocoa supply chain to achieve defined sustainable cocoa objectives

Reduction of free height of fall if starting section is easily accessible unless guarding is provided

or mechanical systems or sources of other radiation

What is BS EN 3060 - Airframe rolling bearings about

– instantaneous water heaters used for showering (IEC 60335‑2‑35)

PD CLC/TS 50131-12 is a standard that covers installed alarm systems that enable the prevention of operator error in alarm applications

the thermal and mechanical responses of the enclosure boundaries and its structure to the fire conditions

BS EN 868-6 is the sixth part of the EN 868 multi-series that discusses packaging for terminally sterilized medical devices

The input voltage to the series circuit is constantly adjusted by the constant current regulator to maintain the series circuit current irrespective of the variations in the load

BS EN 15436-1 is a European Standard that defines terms for road service area maintenance equipment

BS EN IEC 62282‑8‑201 defines the evaluation methods of typical performances for electric energy storage systems using hydrogen

This classification system defines the basic and most important characteristics of industrial wastewater from different dimensions