Автоматические наружные дефибрилляторы HeartStart FRx
Type approval of measuring instruments · reg. No. KZ.02.02.04854-2016
An expired certificate is not a ban. An instrument made in 2016–2021 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.02.02.04854-2016
- Name
- Автоматические наружные дефибрилляторы
- Type, model
- HeartStart FRx
- Manufacturer
- Philips Medical Systems, США
- Certificate holder
- ТОО TND, 050050, г. Алматы, ул. Райымбека, 169/1, тел (727) 2507194, 2507195,
- Type approval certificate
- 12616
- Date of issue
- 09.02.2016
- Valid until
- 09.02.2021
- Verification interval
- 1 год
Record data is shown in the original language (Russian), as in the official register.
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Similar records
Автоматические наружные дефибрилляторы HeartStart FRxKZ.02.01.03801-2026 · фирма «Philips Medical Systems», СШААвтоматические наружные дефибрилляторы HeartStart FRxKZ.02.01.00883-2020 · фирма «Philips Medical Systems»,157,15700,15700000,Нидерланды, Зарубеж, Зарубеж, -Нидерланды, Зарубеж, Зарубеж, -,Дефибрилляторы HeartStart FRXKZ.02.02.01847-2009 · фирма Philips Medical Systems
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.