Системы ультразвуковые диагностические медицинские LOGIQ F3, LOGIQ F6, LOGIQ F8
Type approval of measuring instruments · reg. No. KZ.02.02.05132-2016
An expired certificate is not a ban. An instrument made in 2016–2021 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.02.02.05132-2016
- Name
- Системы ультразвуковые диагностические медицинские
- Type, model
- LOGIQ F3, LOGIQ F6, LOGIQ F8
- Manufacturer
- фирма GE Medical Systems China Co.
- Certificate holder
- ТОО Медико-Инновационные Технологии
- Type approval certificate
- 13141
- Date of issue
- 05.07.2016
- Valid until
- 05.07.2021
- Verification interval
- 2 года
- Verification procedure
- Системы ультразвуковые диагностические медицинские LOGIQ F3, LOGIQ F6, LOGIQ F8, производства фирмы E Medical Systems China Co., Ltd, Китай. 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.