Монитор пациента iM80
Type approval of measuring instruments · reg. No. KZ.02.01.01224-2021
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.02.01.01224-2021
- Name
- Монитор пациента
- Type, model
- iM80
- Manufacturer
- фирма «EDAN Instruments, Inc.», Китай
- Certificate holder
- 081240010645,Товарищество с ограниченной ответственностью FORTIS PAI (ФОРТИС ПАЙ), Казахстан, Алматы г.а., Алмалинская р.а., ул. Жамбыла , к.29,Phone,Email+7 (727) 234 46 44,
- Type approval certificate
- 1224
- Date of issue
- 21.09.2021
- Valid until
- 21.09.2026
- Verification interval
- 1 год
- Verification procedure
- СТ РК 2.367-2015 «ГСИ РК. Мониторы пациента. 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.