ISO/TS 15338:2020 PDF

ISO/TS 15338:2020 PDF

Name:
ISO/TS 15338:2020 PDF

Published Date:
03/01/2020

Status:
Active

Description:

Surface chemical analysis - Glow discharge mass spectrometry - Operating procedures

Publisher:
International Organization for Standardization (Technical Standard)

Document status:
Active

Format:
Electronic (PDF)

Delivery time:
10 minutes

Delivery time (for Russian version):
200 business days

SKU:

Choose Document Language:
$37.2
Need Help?

ISO/TS 15338:2020 gives procedures for the operation and use of glow discharge mass spectrometry (GD-MS). There are several GD-MS systems from different manufacturers in use and this document describes the differences in their operating procedures when appropriate.

NOTE This document is intended to be read in conjunction with the instrument manufacturers' manuals and recommendations.


Edition : 2nd
File Size : 1 file , 1.2 MB
Note : This product is unavailable in Russia, Ukraine, Belarus
Number of Pages : 18
Published : 03/01/2020
Same As : ISO/TS 15338:2020

History

ISO/TS 15338:2020
Published Date: 03/01/2020
Surface chemical analysis - Glow discharge mass spectrometry - Operating procedures
$37.2
ISO/TS 15338:2009
Published Date: 04/01/2009
Surface chemical analysis - Glow discharge mass spectrometry (GD-MS) - Introduction to use
$41.4

Related products

ISO/TS 15338:2020
Published Date: 03/01/2020
Surface chemical analysis - Glow discharge mass spectrometry - Operating procedures
$37.2

Best-Selling Products

MEDDEV 13/93
Published Date:
Guidelines Relating to the Application of: The Council Directive 90/385/EEC on Active Implantable Medical Devices and The Council Directive 93/42/EEC on Medical Devices
MEDDEV 2.1/3
Published Date: 03/01/1998
Guidelines Relating to the Demarcation Between 90/385/EEC on Active Implatable Medical Devices, 93/42/EEC on Medical Devices,65/65/EEC Relating to Medicinal Products & Related Directives
MEDDEV 3/94
Published Date: 04/01/1994
Guidelines Relating to the Application of : The Council Directive 90/385/EEC on Active Implantable Medical Devices and The Council Directive 93/42/EEC on Medical Devices