Системы ультразвуковые диагностические ClearVue 850 с принадлежностями
Type approval of measuring instruments · reg. No. KZ.02.02.05518-2017
An expired certificate is not a ban. An instrument made in 2017–2022 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.02.02.05518-2017
- Name
- Системы ультразвуковые диагностические
- Type, model
- ClearVue 850 с принадлежностями
- Manufacturer
- фирма Philips Healthcare (Suzhou) Co.
- Certificate holder
- ТОО TND
- Type approval certificate
- 13901
- Date of issue
- 10.03.2017
- Valid until
- 10.03.2022
- Verification interval
- 2 года
- Verification procedure
- Система ультразвуковая диагностическая ClearVue 850 с принадлежностями, производства фирмы Philips Healthcare (Suzhou) 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.
Similar records
Системы ультразвуковые диагностических ClearVue 850 с принадлежностямиKZ.02.01.01568-2022 · фирмы «Philips Healthcare (Suzhou) Co., Ltd», Китай ,Қытай, Philips Healthcare (Suzhou) Co., Ltd фирмасы,045,04500,04500000AdrAdrEngСистемы ультразвуковые диагностические ClearVue варианты исполнения ClearVue 350, ClearVue 550KZ.02.01.00850-2020 · фирма «Philips Healthcare (Suzhou) Co., Ltd.», Китай
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.