Buy EN NON-DESTRUCTIVE TESTING – CHARACTERIZATION AND VERIFICATION OF ULTRASONIC EXAMINATION EQUIPMENT – PART 2. 10 Mar Denna standard ersätter SS-EN , utgåva 1 och SS-EN The European Standard EN has the status of a Swedish. 8 Jun The European Standard EN has the status of a Swedish Standard. This document con- tains the official English version of EN.

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Learn more about the cookies we use and how to change your settings. Customers who bought this product also bought BS EN Characterization and verification of ultrasonic examination equipment.

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Probes BS EN is a European Standard which covers probes used for ultrasonic non-destructive examination in the following categories with centre frequencies in the range 0,5 MHz to 15 MHz, focusing and without focusing means: Worldwide Standards We can source any standard from anywhere in the world.

Specification for calibration block No. Accept and continue Learn more about the cookies we use and how to change your settings. Routine tests for the verification of probes using on-site methods are given in EN Periodic tests for probes are not included in this document.

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Your basket is empty. Foreword 1 Scope 2 Normative references 3 Terms and definitions 4 General requirements for compliance 5 Technical specification for probes 12668-22 Test equipment 7 Performance requirements for probes Annex A normative Calculation of near field length of non-focusing probes Annex B informative Calibration block for angle-beam probes Bibliography.

BS EN 12668-2:2010

Click to learn more. BS EN is a European Standard which covers probes used for ultrasonic non-destructive examination in the following categories with centre frequencies in the range 0,5 MHz to 15 MHz, focusing and without focusing means:.

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Contents 16268-2 BS EN Find Similar Items This product falls into the following categories. If parameters in addition to those specified in EN are to be verified during the probe’s life time, as agreed upon by the contracting parties, the methods of verification for these additional parameters should be selected from those given in this document. Take the smart route to manage medical device compliance. This website wn best viewed with browser version of up to Microsoft Internet Explorer 8 or Firefox 3.