Автоматические наружные дефибрилляторы BeneHeart в вариантах исполнениях BeneHeart C1 Fully Automatic, BeneHeart C1 А Fully Automatic, BeneHeart С2 Fully Automatic, BeneHeart С2А Fully Automatic, BeneHeart S1 Fully Automatic, BeneHeart S1 А Fully Automatic, BeneHeart S2 Fully Automatic, BeneHeart S2A Fully Automatic в комплекте с принадлежностями
Type approval of measuring instruments · reg. No. KZ.02.01.03439-2025
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.02.01.03439-2025
- Name
- Автоматические наружные дефибрилляторы
- Type, model
- BeneHeart в вариантах исполнениях BeneHeart C1 Fully Automatic, BeneHeart C1 А Fully Automatic, BeneHeart С2 Fully Automatic, BeneHeart С2А Fully Automatic, BeneHeart S1 Fully Automatic, BeneHeart S1 А Fully Automatic, BeneHeart S2 Fully Automatic, BeneHeart S2A Fully Automatic в комплекте с принадлежностями
- Manufacturer
- фирма «Shenzhen Mindray Bio-Medical Electronics Co., Ltd.», Китай
- Country
- Китай
- Certificate holder
- ТОО «MedLicense»
- Type approval certificate
- 3439
- Date of issue
- 21.08.2025
- Valid until
- 21.08.2030
- Verification interval
- 1 год
- Verification procedure
- СТ РК 2.566-2018 «Дефибрилляторы 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.