Система медицинская ультразвуковая диагностическая M-Turbo

Type approval of measuring instruments · reg. No. KZ.02.01.00866-2020

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.02.01.00866-2020
Name: Система медицинская ультразвуковая диагностическая
Type, model: M-Turbo
Manufacturer: «FUJIFILM SonoSite, Inc.», США
Certificate holder: 120140010609,Товарищество с ограниченной ответственностью НаноФарм, Казахстан, Алматы г.а., Бостандыкская р.а., Улица Экспериментальная База, 3а.+7 (727) 393 68 34,Email-}
Type approval certificate: 866
Date of issue: 06.01.2021
Valid until: 06.01.2026
Verification interval: 2 года
Verification procedure: - KZ.04.02.09306 - 2015 «Системы медицинские ультразвуковые диагностические M-Turbo, производства фирмы FUJIFILM SonoSite, Inc., США. Методика поверки» - СТ РК 2.379 - 2015 «ГСИ РК. АППАРАТЫ УЛЬРАЗВУКОВЫЕ ДИАГНОСТИЧЕСКИЕ. 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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