Системы внутрисосудистого введения рентгеноконтрастного вещества Illumena Nео
Type approval of measuring instruments · reg. No. KZ.02.01.02981-2024
Instruments of this type are listed in the GSI register of Kazakhstan and can be verified in Kazakhstan. Verification interval: 2 года.
Record data
- Registration number
- KZ.02.01.02981-2024
- Name
- Системы внутрисосудистого введения рентгеноконтрастного вещества
- Type, model
- Illumena Nео
- Manufacturer
- фирма «Liebel-Flarsheim Company LLC», США
- Country
- США
- Certificate holder
- ТОО «МЕДИЛЮКС»
- Type approval certificate
- 2981
- Date of issue
- 05.01.2025
- Valid until
- 05.01.2030
- Verification interval
- 2 года
- Verification procedure
- KZ.05.01.00572-2020 «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.
Need verification of an instrument of this type?
We will find an accredited laboratory in your region by scope of accreditation — range and accuracy class. One request instead of calling around.
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.