Анализатор дефибрилляторов типа Impulse 6000D, производства Fluke Biomedical, США. Методика поверки.

Verification procedures for measuring instruments · reg. No. KZ.04.02.08570-2014

Verification procedure registered in the GSI register of Kazakhstan

Measuring instruments whose type approval certificate names this procedure are verified according to it.

Record data

Registration number: KZ.04.02.08570-2014
Procedure: Анализатор дефибрилляторов типа Impulse 6000D, производства Fluke Biomedical, США. Методика поверки.
Registration date: 13.06.2014
Year of development: 2014
Developer: ТОО Казахстанский центр поверки и сертификации, согл. с РГП КазИнМетр
Approved by: ТОО Казахстанский центр поверки и сертификации
Decision: № 486 dated 13.06.2014

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.