AS NZS 3551 PDF

Outlines procedures required to develop management programs for medical equipment. These include protocols and procedures for. Testing to AS/NZS is neither relevant nor necessary in aged care facilities unless the equipment is part of a facility that is intended to be. in AS/NZS In-service safety inspection and testing of electrical equipment. AS/NZS Management programs for medical devices provides.

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Follow these links to find other Standards similar to the one you are viewing. Citations This document is cited by New Zealand legislation. Physical Inspection Check for signs of damage Check that aas device is clean B. Management of aas Parameters are determined at time of device acceptance in accordance with manufacturers’ specification. Electricity Safety Regulations Ministry: Expand the box to see details.

It is all about risk management, health and safety and ultimately “peace of mind”. The person must test the appliance and either This document may make references to other documents.

Ensuring you get the right Service Technician is critical to ensure correct compliance. What is the Standard about?

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AED Performance Verification AS/NZS 3551

Other people who purchased this product also bought One of the key purposes of this act is to provide a balanced framework to ensure the health and safety of workers and workplaces by “protecting workers and other persons against harm to their health by eliminating or minimising risks arising from work or from potential ass risk plant”. It is designed to cover every economic sector and virtually every activity of the humankind where technical standards may be used.

A used appliance that is sold or offered for sale is deemed to be electrically safe if, at the time it is sold or offered for sale, Risk also exists where not all required electrical and performance tests have been completed. The testing they do is normally hzs for fridges and microwaves but not for medical equipment.

These include protocols and procedures for procurement, acceptance, maintenance activities throughout the service life of the medical equipment, and finally disposal of medical equipment. General requirements for basic safety and essential performance ISO Medical devices – Application of risk management to medical devices AS ISO Medical devices—Quality management systems – Requirements for regulatory purposes.

The technician will maintain the full suite of testing equipment to ensure that all necessary tests are undertaken for both electrical safety and performance checking that the devices work correctly. References This document may make references to other documents.

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Physical Inspection Check for signs of damage Check that the device is clean.

Testing of medical devices is normally undertaken by a professional biomedical technician. Sustaining business, sustaining life.

Standards New Zealand :: Management programs for medical equipment

Correct performance verification is critical to ensure safe use of the medical device for the patient and the operator. Despite anything nsz these regulations, the following installations, fittings, and appliances are deemed to be electrically safe if they comply with the standards indicated and are used in accordance with those standards: Schedule 2 Citation Context: Qs procedures required to develop management programs for medical equipment.

Medical devices are a specialist area which is subject to particular standards and legislation. Click Buy for Online Library subscription. All referenced documents are displayed below.

International Classification for Standards ICS is an international classification system for technical standards.