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Анализатор автоматический клинический химии и иммунологии Dimension Xpand Plus в комплекте с принадлежностями, производства Siemens Healthcare Diagnostics Inc., США. Методика поверки.

Verification procedures for measuring instruments · reg. No. KZ.04.02.08317-2014

Verification procedure registered in the GSI register of Kazakhstan

Measuring instruments whose type approval certificate names this procedure are verified according to it. The procedure text is attached.

Record data

Registration number
KZ.04.02.08317-2014
Procedure
Анализатор автоматический клинический химии и иммунологии Dimension Xpand Plus в комплекте с принадлежностями, производства Siemens Healthcare Diagnostics Inc., США. Методика поверки.
Registration date
31.03.2014
Year of development
2013
Developer
ЮКФ РГП КазИнМетр согл. с ТОО Siemens
Approved by
РГП КазИнМетр
Decision
№ 285 dated 31.03.2014
File
Open the procedure PDF

Record data is shown in the original language (Russian), as in the official register.

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Source: GSI register of Kazakhstan, techreg.gov.kz, copy of 26.09.2026. The information is for reference — always confirm against the register and the instrument documents.