Информационный центр наблюдения за пациентом Philips IntelliVue в комплекте, производства фирмы Philips Medical Systems, США Методика поверки
Verification procedures for measuring instruments · reg. No. KZ.04.02.04261-2009
Measuring instruments whose type approval certificate names this procedure are verified according to it.
Record data
- Registration number
- KZ.04.02.04261-2009
- Procedure
- Информационный центр наблюдения за пациентом Philips IntelliVue в комплекте, производства фирмы Philips Medical Systems, США Методика поверки
- Registration date
- 04.09.2009
- Year of development
- 2009
- Developer
- ЮКФ РГП КазИнМетр, согласовано с ТОО TND
- Approved by
- РГП КазИнМетр
- Decision
- № 661 dated 04.09.2009
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.