ISO 22442-3 PDF

It is most important that the objectives and potential uses of an. AAMI product standard or recommended practice are clearly understood. The objectives of. INTERNATIONAL. STANDARD. ISO. First edition. Medical devices utilizing animal tissues and their derivatives —. Part 3: Validation of the. Permission can be requested from either ISO at the address below or ISO’s .. ISO , Medical devices utilizing animal tissues and their.

Author: Kigarg Tygoktilar
Country: Burkina Faso
Language: English (Spanish)
Genre: Career
Published (Last): 23 November 2006
Pages: 115
PDF File Size: 18.65 Mb
ePub File Size: 1.32 Mb
ISBN: 111-5-66261-658-4
Downloads: 56006
Price: Free* [*Free Regsitration Required]
Uploader: Motaxe

For this reason, the following need to be considered in particular: Ministry of Commerce and Industry. Find Similar Items This product falls into the following categories. Conventional processes used for sterilization, when used for the treatment of animal tissues for medical devices, have not been shown to be completely effective in inactivating the causative agents of transmissible spongiform encephalopathy.

Your basket is empty.

The guidance given in this standard is not normative and is not provided as a checklist for auditors. Definition of the process es and materials to be used Adequate inactivation validation before routine use Performance monitoring of the process during manufacture Appropriate equipment maintenance Staff training.

Medical devices utilizing animal tissues and their derivatives — Part 3: For this reason, evaluation of the manufacturing process can provide a measure of confidence that a wide number of viruses, including unknown pathogenic viruses are eliminated. This part of ISO does not specify a quality management system for the control of all stages of production of medical devices.

Requirements for regulatory purposes. Tierische Gewebe und deren Derivate, die zur Herstellung von Medizinprodukten eingesetzt werden.

  2008 HONDA ACCORD MAINTENANCE MANUAL PDF

BS EN ISO 22442-3:2007

This part of ISO does not cover the utilization of isl tissues in medical devices. Learn more about the cookies we use and how to change your settings.

Attention is drawn to the standards for quality management systems see BS EN ISO that control all stages of production or reprocessing of medical devices. For this reason, the following need to be considered in particular:.

NOTE 3 It is not a requirement of this part of ISO to have a full quality management system during manufacture, but it does specify requirements for some of the elements of a quality management system.

GSO ISO – Standards Store – GCC Standardization Organization

This website is best viewed with browser version of up to Microsoft Internet Explorer 8 or Firefox 3. The files of this standards is not available in the store right now. Please download Chrome or Firefox or view our browser tips.

For the safety of medical devices there are two complementary approaches see BS EN ISO that can be adopted to control the potential contamination of tissues. Similar principles may apply to TSE agents. Accept and continue Learn more about the cookies we use and how to change your settings. The standards for quality management systems recognize that, for certain processes used in manufacturing, the effectiveness of that process cannot be fully verified by subsequent inspection and testing of the product.

It is not a requirement of this part of BS EN ISO to have a full quality management system during manufacture, but it does specify requirements for some of the elements of a quality management system. Medical devices utilizing animal tissues and their derivatives.

It does not cover other transmissible and non-transmissible agents. Worldwide Standards We can source any standard from anywhere in the world. Attention is drawn to the standards for quality management systems see ISO that control all stages of production or reprocessing of iao devices.

  KASTURIRANGAN COMMITTEE REPORT MALAYALAM PDF

You may experience issues viewing this site in Internet Explorer 9, 10 or It does not cover other transmissible and non-transmissible agents.

The quality management system elements that are required 22424-3 this part of ISO can form part of a quality management system conforming to ISO We use cookies to make our website easier to use and to better understand your needs.

Saudi Standards, Metrology and Quality Organization. This part of BS EN ISO does not cover the utilization of human tissues in medical devices, nor does it specify a quality management system for the control of all stages of production of medical devices. Conventional processes used for sterilization, when used for the treatment of animal tissues for medical devices, have not been shown to be completely effective in inactivating the causative agents of transmissible spongiform encephalopathy.

Search all products by. You may find similar items within these categories by selecting from the choices below:. Click to learn more.

You can buy this standard from any national standardization body. Take the smart route to manage medical device compliance. It applies where required by the risk management process as described in ISO Historically there have been many instances of unknown or unsuspected viral contamination during manufacture.

Author: admin