Автоматические наружные дефибрилляторы HeartStart FRx

Type approval of measuring instruments · reg. No. KZ.02.01.00883-2020

Archived record: the certificate was valid 2021–2026

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.02.01.00883-2020
Name: Автоматические наружные дефибрилляторы
Type, model: HeartStart FRx
Manufacturer: фирма «Philips Medical Systems»,157,15700,15700000,Нидерланды, Зарубеж, Зарубеж, -Нидерланды, Зарубеж, Зарубеж, -,
Certificate holder: 030440003414,Товарищество с ограниченной ответственностью TND,SearchItemTextТоварищество с ограниченной ответственностью TND,SearchItemId030440003414030440003414,Товарищество с ограниченной ответственностью TND118,11816,11816207,Проспект Райымбека, 169.,Казахстан, Алматы г.а., Жетысуская р.а., Проспект Райымбека, 169.+7 (727) 250 71 94,Emailinfo@tnd.kz}
Type approval certificate: 883
Date of issue: 29.01.2021
Valid until: 29.01.2026
Verification interval: 1 год
Verification procedure: KZ.04.02.10075-2016 «Автоматические наружные дефибрилляторы HeartStart FRx. Методика поверки».

Record data is shown in the original language (Russian), as in the official register.

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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.

Record data

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