Standard BS EN 13458-1:2002 1.7.2002 - Cryogenic vessels. Static vacuum insulated vessels. Fundamental requirements. (Kryogenické nádoby - Stabilní
BS EN 13458-2:2002 Cryogenic vessels - Static vacuum insulated vessels. Design, fabrication, inspection and testing (incorporating corrigendum No. 1)
This is a multi-part document divided into the following parts: Part 1 Cryogenic vessels.Static vacuum insulated vessels. Fundamental requirements; Part 2 Cryogenic vessels.Static vacuum insulated vessels. BS EN ISO 13485:2016: Title: Medical devices. Quality management systems. Requirements for regulatory purposes: Status: Current, Work in hand: Publication Date: 29 February 2016: Normative References(Required to achieve compliance to this standard) EN ISO 9000:2015, ISO 9000:2015: Informative References(Provided for Information) This standard BS EN 13458-2:2002 Cryogenic vessels.
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Requirements for regulatory purposes. Published 24-Jul-2003. ISBN: 9780580686689 BS EN ISO 13485:2003 is maintained by CH/210/1. This standard is available from the following sources: British Standards Shop (Shop) British Standards Online (BSOL) DIN EN 13458-2 - 2003-02 Cryogenic vessels - Static vacuum insulated vessels - Part 2: Design, fabrication, inspection and testing; German version EN 13458-2:2002. This part of ISO 21009 specifies operational requirements for static vacuum insulated vessels designed for a maximum allowable pressure of more than 50 kPa (0,5 bar). It may also be used as a guideline for vessels designed for a maximum allowable pressure of less than 50 kPa (0,5 bar).
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Part 3 Aseptic processing of health care products. Lyophilization. Part 4 Aseptic processing of health care products. Clean-in-place technologies.
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Title. Cryogenic vessels. Static vacuum insulated vessels. Design, fabrication, inspection and testing. Status. Confirmed, Current. Publication Date.
Medicinskt tillstånd
BS EN ISO 13485:2016: Title: Medical devices. Quality management systems. Requirements for regulatory purposes: Status: Current, Work in hand: Publication Date: 29 February 2016: Normative References(Required to achieve compliance to this standard) EN ISO 9000:2015, ISO 9000:2015: Informative References(Provided for Information) This standard BS EN 13458-2:2002 Cryogenic vessels. Static vacuum insulated vessels is classified in these ICS categories: 23.020.40 Cryogenic vessels ISO 13458 Design and Manufacture of Medical Devices Standard This standard covers the requirements for a comprehensive management system for the design and manufacture of medical devices. If you wish to find out more about ISO 13458 please contact us today.
More details Print $78.85-60%. $197.12. Quantity. Add to cart.
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This is a multi-part document divided into the following parts: Part 1 Aseptic processing of health care products. General requirements. Part 2 Aseptic processing of health care products. Filtration. Part 3 Aseptic processing of health care products. Lyophilization. Part 4 Aseptic processing of health care products. Clean-in-place technologies.
ISO 13458 . Design and Manufacture of Medical Devices Standard – Looks at set requirements for the design and manufacturing of medical devices. For more information on ISO 13458 please contact IQS EN 13458-2:2002 (E) 3 Foreword This document (EN 13458-2:2002) has been prepared by Technical Committee CEN/TC 268 "Cryogenic vessels", the secretariat of which is held by AFNOR. This European Standard shall be given the status of a national standard, either by publication of an identical text or ISO 13485:2016 specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements.
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BS EN 13458-2:2002. Title. Cryogenic vessels. Static vacuum insulated vessels. Design, fabrication, inspection and testing. Status. Confirmed, Current. Publication Date. 29 November 2002.
To learn more and buy, click HERE. What is this standard about? This is the internationally recognized quality management system (QMS) standard for the medical device industry.
Technical Barriers to Trade (TBT) see the following URL: www.iso. org/iso/foreword.html. The committee responsible for this document is Technical Committee ISO/TC210, Quality management and corresponding general aspects for medical devices. This third edition of ISO 13485 cancels and replaces the second edition (ISO 13485:2003) and
Status.
Standards are often used as the basis for contracts between businesses. BS EN 13458-3 is maintained by PVE/18. The current release of this standard is: BS EN 13458-3:2003 Cryogenic vessels. Static vacuum insulated vessels. BS EN ISO 13485:2003.