Аппараты для заместительной почечной терапии PrisMax
Type approval of measuring instruments · reg. No. KZ.02.01.03479-2025
Instruments of this type are listed in the GSI register of Kazakhstan and can be verified in Kazakhstan. Verification interval: 1 год.
Record data
- Registration number
- KZ.02.01.03479-2025
- Name
- Аппараты для заместительной почечной терапии
- Type, model
- PrisMax
- Manufacturer
- фирма «Baxter Healthcare S.A.», Швейцария на производственной площадке фирмы «Gambro Dasco S.p.A.», Италия
- Country
- Италия
- Certificate holder
- ТОО «Mitek Almaty» (Митек Алматы)
- Type approval certificate
- 3479
- Date of issue
- 02.09.2025
- Valid until
- 02.09.2030
- Verification interval
- 1 год
- Verification procedure
- «Аппараты для заместительной почечной терапии PrisMax. 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.