Аппарат искусственной вентиляции легких передвижных Elisa 600, Elisa 800, Elisa 800 VIT с принадлежностями
Type approval of measuring instruments · reg. No. KZ.02.01.00456-2020
An expired certificate is not a ban. An instrument made in 2020–2025 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.02.01.00456-2020
- Name
- Аппарат искусственной вентиляции легких передвижных
- Type, model
- Elisa 600, Elisa 800, Elisa 800 VIT с принадлежностями
- Manufacturer
- «Lowenstein Medical GmbH & Co. KG», Германия
- Certificate holder
- Товарищество с ограниченной ответственностью НаноФарм, 050060, Республика Казахстан, г. Алматы, ул. Экспериментальная база 3а, тел: 8 (727) 393 6834,Emai: linfo@nanopharm.kz
- Type approval certificate
- 456
- Date of issue
- 20.01.2020
- Valid until
- 20.01.2025
- Verification interval
- ДваГода
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.