Инжекторы для введения контрастных веществ модели: OptiStar LE, CT 9000 ADV, Angiomat Illumena, Optistar Elite, производства Liebel- Flarsheim (Mallinckrodt Inc.) LLC, США Методика поверки.
Verification procedures for measuring instruments · reg. No. KZ.04.02.06332-2012
Measuring instruments whose type approval certificate names this procedure are verified according to it. The procedure text is attached.
Record data
- Registration number
- KZ.04.02.06332-2012
- Procedure
- Инжекторы для введения контрастных веществ модели: OptiStar LE, CT 9000 ADV, Angiomat Illumena, Optistar Elite, производства Liebel- Flarsheim (Mallinckrodt Inc.) LLC, США Методика поверки.
- Registration date
- 28.02.2012
- Year of development
- 2012
- Developer
- ЮКФ РГП КазИнМетр согласовано с ТОО МЕДИЛЮКС
- Approved by
- РГП КазИнМетр
- Decision
- 28.02.2012
- 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.