Мониторы фетальные серии F, исполнения F30, F50, F80, F90, WF100
Type approval of measuring instruments · reg. No. KZ.02.01.00944-2021
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.02.01.00944-2021
- Name
- Мониторы фетальные
- Type, model
- серии F, исполнения F30, F50, F80, F90, WF100
- Manufacturer
- Guangdong Biolight Meditech Co.,Ltd045,04500,04500000,Китай, Зарубеж, Зарубеж, -,
- Certificate holder
- 000640005130,Товарищество с ограниченной ответственностью ИНФРАДИНSearchItemTextТоварищество с ограниченной ответственностью ИНФРАДИН,SearchItemId000640005130}118,11815,11815199,Г.НУР-СУЛТАН, РАЙОН АЛМАТЫ, УЛИЦА 23-15, Д 11, КВ 170,+7 (717) 231 11 09,Email2019315@mail.ru,
- Type approval certificate
- 944
- Date of issue
- 11.03.2021
- Valid until
- 11.03.2026
- Verification interval
- 1 год
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.