Автоматические нефелометры BN ProSpecв комплекте с принадлежностями и реагентами
Type approval of measuring instruments · reg. No. KZ.02.02.04195-2014
An expired certificate is not a ban. An instrument made in 2014–2019 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.02.02.04195-2014
- Name
- Автоматические нефелометры
- Type, model
- BN ProSpecв комплекте с принадлежностями и реагентами
- Manufacturer
- Siemens Healthcare Diagnostics Productd GmbH, Германия(держатель лицензии - Siemens Healthcare Diagnostics Inc., Соединенные Штаты Америки
- Certificate holder
- ТОО Вика Плюс, РК, 110007, Костанайская область, г. Костанай, ул. О. Шипина 170-4,тел. +7 (7142) 578103, 8777 2747669, e-mail nataxa4er@mail.ru,
- Type approval certificate
- 11109
- Date of issue
- 10.10.2014
- Valid until
- 10.10.2019
- Verification interval
- 1 год
- Verification procedure
- Автоматический нефелометр BN ProSpec в комплекте с принадлежностями и реагентами. 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.