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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Standard & Legislation – Biomedical Services NZ Ltd
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, Citations This document is cited by New Zealand ae. Medical devices are a specialist area which is subject to particular standards and legislation.
International Classification for Standards ICS is an international classification system for technical standards.
Correct performance verification is critical to ensure safe use of the medical device for the patient and the operator.
Follow these links to find other Standards similar to the one you are viewing.
AED Performance Verification
Physical Inspection Check for signs of damage Check that the device is clean B. 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 high risk plant”.
Other people who purchased this product also bought Parameters are ae at time of device acceptance in accordance with manufacturers’ specification. Schedule 2 Citation Context: Testing of medical devices is normally undertaken by a professional biomedical technician.
The testing they do is normally suitable aas fridges and microwaves but not for medical equipment. Outlines procedures required to develop management programs for medical equipment. Ensuring you get the right Service Technician is critical to ensure correct compliance.
Physical Inspection Check for signs of damage Check that the device is clean.
These include protocols and procedures for procurement, acceptance, maintenance activities throughout the service life of the medical equipment, and finally disposal of medical equipment.
What is the Standard about? This document may make references to other documents. 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 person must test the appliance and either All referenced documents are displayed below.
Click Buy for Online Library subscription. Electricity Safety Regulations Ministry: Despite anything in 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: The technician will maintain the full suite ass testing equipment to ensure that all necessary tests are undertaken for both electrical safety and performance checking that the devices work correctly.
Nzss is designed to cover every economic sector and virtually every activity of the humankind where technical standards may be used. Management of stock Expand the box to see details.
AED Performance Verification AS/NZS 3551
Sustaining business, sustaining life. Risk also exists where not all nze electrical and performance tests have been completed. References This document may make references to other documents.
It is all about risk management, health and safety and ultimately “peace of mind”.