Система внутрисосудистого введения рентгеноконтрастного вещества Illumena NEO
Type approval of measuring instruments · reg. No. KZ.02.01.00522-2020
An expired certificate is not a ban. An instrument made in 2020–2025 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.02.01.00522-2020
- Name
- Система внутрисосудистого введения рентгеноконтрастного вещества
- Type, model
- Illumena NEO
- Manufacturer
- фирма Liebel-Flarsheim Company LLC,США
- Certificate holder
- Товарищество с ограниченной ответственностью МЕДИЛЮКС, Казахстан, Алматы г.а., Медеуская р.а., улица Курмангазы, 48 а, кв 407, 409+7 (727) 234 78 86,Email7272347886}
- Type approval certificate
- 522
- Date of issue
- 21.02.2020
- Valid until
- 21.02.2025
- Verification interval
- 2 года
- Verification procedure
- «Системы внутрисосудистого введения рентгеноконтрастного вещества Illumena NEO, производства фирмы «Liebel-Flarsheim Company LLC», США. Методика поверки»
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.