Система ультразвуковая диагностическая ClearVue варианты исполнения ClearVue 350, ClearVue 550
Type approval of measuring instruments · reg. No. KZ.02.02.03367-2013
An expired certificate is not a ban. An instrument made in 2013–2018 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.02.02.03367-2013
- Name
- Система ультразвуковая диагностическая
- Type, model
- ClearVue варианты исполнения ClearVue 350, ClearVue 550
- Manufacturer
- фирма "Philips Ultrasound, Inc", США
- Certificate holder
- ТОО "TND"
- Type approval certificate
- 9227
- Date of issue
- 18.04.2013
- Valid until
- 18.04.2018
- Verification interval
- 2 года
- Verification procedure
- Система ультразвуковая диагностическая ClearVue варианты исполнения ClearVue 350, ClearVue 550, производства фирмы Philips Ultrasound, Inc, США. Методика поверки.
Record data is shown in the original language (Russian), as in the official register.
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Similar records
Системы ультразвуковые диагностические ClearVue варианты исполнения ClearVue 350, ClearVue 550KZ.02.01.00850-2020 · фирма «Philips Healthcare (Suzhou) Co., Ltd.», КитайСистемы ультразвуковые диагностические ClearVue варианты исполнения ClearVue 350, ClearVue 550KZ.02.02.04728-2015 · 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.