Системы мониторинга внутричерепного давления PRESSIO 2
Type approval of measuring instruments · reg. No. KZ.02.01.01229-2021
An expired certificate is not a ban. An instrument made in 2021–2026 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.02.01.01229-2021
- Name
- Системы мониторинга внутричерепного давления
- Type, model
- PRESSIO 2
- Manufacturer
- фирма Sophysa SA, Франция
- Certificate holder
- 120140010609,Товарищество с ограниченной ответственностью НаноФарм, Казахстан, Алматы г.а., Ауэзовская р.а., УЛИЦА ЭКСПЕРИМЕНТАЛЬНАЯ БАЗА, 3А,Phone,Email+7 (727) 393 68 34,
- Type approval certificate
- 1229
- Date of issue
- 24.09.2021
- Valid until
- 24.09.2026
- Verification interval
- 2 года
- Verification procedure
- "Системы мониторинга внутричерепного давления PRESSIO 2, производства фирмы "Sophysa SA", Франция. 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.