Системы ультразвуковые диагностические медицинские серии LOGIQ модели LOGIQ E10, LOGIQ E10S, LOGIQ P8, LOGIQ P10 с принадлежностями
Type approval of measuring instruments · reg. No. KZ.02.01.01644-2022
Instruments of this type are listed in the GSI register of Kazakhstan and can be verified in Kazakhstan. Verification interval: 1 год.
Record data
- Registration number
- KZ.02.01.01644-2022
- Name
- Системы ультразвуковые диагностические медицинские
- Type, model
- серии LOGIQ модели LOGIQ E10, LOGIQ E10S, LOGIQ P8, LOGIQ P10 с принадлежностями
- Manufacturer
- «GE Ultrasound Korea Ltd», Корея,Корея, «GE Ultrasound Korea Ltd» ,114,11400,11400000,-AdrAdrEng
- Certificate holder
- ТОО «Медико-Инновационные Технологии»,Медико-Инновациялық Технологиялар ЖШС,118,11816,11816201,УЛИЦА НАУРЫЗБАЙ БАТЫРА, 8AdrAdrEng+7 (727) 347 00 03,
- Type approval certificate
- 1644
- Date of issue
- 22.07.2022
- Valid until
- 22.07.2027
- Verification interval
- 1 год
- Verification procedure
- СТ РК 2.379-2015 «ГСИ РК Аппараты ультразвуковые диагностические. 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.