Системы диагностические ультразвуковые стационарные HERA I10
Type approval of measuring instruments · reg. No. KZ.02.01.00513-2020
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.02.01.00513-2020
- Name
- Системы диагностические ультразвуковые стационарные
- Type, model
- HERA I10
- Manufacturer
- Samsung Medison Co., Ltd, Южная Корея
- Certificate holder
- Акционерное общество Ordamed,г. Алматы ,ул. Дуйсенова, 25, кабинет 202, +7 (727) 270 70 72,Emailinfo@ordamed.kz,
- Type approval certificate
- 513
- Date of issue
- 14.02.2020
- Valid until
- 14.02.2025
- Verification interval
- 2 года
- Verification procedure
- "Системы диагностические ультразвуковые стационарные HERA I10, производства "Samsung Medison Co., Ltd", Южная Корея. 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.