Мониторы пациента P, исполнения P1, P12, P15, P18, P22
Type approval of measuring instruments · reg. No. KZ.02.01.01668-2022
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.02.01.01668-2022
- Name
- Мониторы пациента
- Type, model
- P, исполнения P1, P12, P15, P18, P22
- Manufacturer
- фирма «Guangdong Biolight Meditech Co., Ltd», Китай,Қытай, Guangdong Biolight Meditech Co., Ltd045,04500,04500000,-AdrAdrEng
- Certificate holder
- ТОО «Инфрадин»,Инфрадин ЖШС,118,11815,11815199,УЛИЦА АХМЕТ БАЙТҰРСЫНҰЛЫ, ДОМ 37, Н. П. 23AdrAdrEng+7 (717) 249 95 27,
- Type approval certificate
- 1668
- Date of issue
- 08.08.2022
- Valid until
- 08.08.2027
- 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.