31 Dec 2015 BS EN ISO 21028-2:2018 BS EN 13458-1:2002 BS EN ISO 21009-2:2015 specifies operational requirements for static vacuum insulated

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

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BS EN 13458-3 : Cryogenic vessels Static vacuum insulated vessels Part 3: Operational requirements.

For more information on ISO 13458 please contact IQS. Head Office: IQS Audits Limited, , 87 North Road, Poole, Dorset, England, BH14 0LT - Phone: +44 (0)1202 973060. Contact us.

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).

BS EN ISO 4032: 2001 Table 1 Preferred sizes Dimensions in mm . … This is a multi-part document divided into the following parts: Part 1 Technical product documentation (TPD).General principles of representation.

12.8.2016 EN 13458-2:2002/AC:2006. 12.8.2016 IEC 60601-1:2005/A1:2012. 10.7.2015. Pilotstyrda säkerhetsventiler (ISO 4126-4:2013). 12.8.2016 EN 13458-2:2002/AC:2006. 12.8.
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BS EN ISO 13485:2016: Title: Medical devices. Quality management systems.

Fundamental requirements; Part 2 Cryogenic vessels.Static vacuum insulated vessels. BS EN ISO 13485:2016: Title: Medical devices.
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1 Mar 2016 The procedures used to develop this document and those intended for its further maintenance are described in the ISO/IEC Directives, Part 1. In

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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.

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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.

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