Инжекторы для введения контрастных веществ модели OptiVantage DH, OptiStar LE, CT 9000 ADV, Angiomat Illumena, Optistar Elite
Type approval of measuring instruments · reg. No. KZ.02.02.02848-2012
An expired certificate is not a ban. An instrument made in 2012–2017 is verified under this type approval: the register keeps archived records precisely for such cases. Check the year of manufacture on the nameplate or in the instrument passport.
Record data
- Registration number
- KZ.02.02.02848-2012
- Name
- Инжекторы для введения контрастных веществ
- Type, model
- модели OptiVantage DH, OptiStar LE, CT 9000 ADV, Angiomat Illumena, Optistar Elite
- Manufacturer
- фирма Liebel- Flarsheim (Mallinckrodt Inc.) LLC
- Certificate holder
- ТОО МЕДИЛЮКС
- Type approval certificate
- 8020
- Date of issue
- 28.02.2012
- Valid until
- 28.02.2017
- Verification interval
- 2 года
Record data is shown in the original language (Russian), as in the official register.
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Similar records
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.