Certera

Дефибрилляторы HeartStartFR3

Type approval of measuring instruments · reg. No. KZ.02.01.00331-2019

Archived record: the certificate was valid 2019–2024

An expired certificate is not a ban. An instrument made in 2019–2024 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.02.01.00331-2019
Name
Дефибрилляторы
Type, model
HeartStartFR3
Manufacturer
«Philips Medical Systems»,223,22300,22300000,США, Зарубеж, Зарубеж, -США, Зарубеж, Зарубеж, -,
Certificate holder
030440003414,Товарищество с ограниченной ответственностью TND,SearchItemTextТоварищество с ограниченной ответственностью TND,SearchItemId030440003414030440003414,Товарищество с ограниченной ответственностью TND118,11816,11816207,г. АЛМАТЫ, ЖЕТЫСУСКИЙ РАЙОН, ПРОСПЕКТ РАЙЫМБЕКА, 169,Казахстан, Алматы г.а., Жетысуская р.а., г. АЛМАТЫ, ЖЕТЫСУСКИЙ РАЙОН, ПРОСПЕКТ РАЙЫМБЕКА, 169+7 (727) 250 71 94,Emailinfo@tnd.kz}
Type approval certificate
331
Date of issue
15.10.2019
Valid until
15.10.2024
Verification interval
1 год
Verification procedure
"Дефибрилляторы HeartStart FR3, производства фирмы Philips Medical Systrms, США. Методика поверки"

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

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Similar records

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.