Дефибрилляторы портативные двухфазные серии Cardiolife модель TEC-7721K
Type approval of measuring instruments · reg. No. KZ.02.02.01432-2008
An expired certificate is not a ban. An instrument made in 2008–2013 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.02.02.01432-2008
- Name
- Дефибрилляторы портативные двухфазные
- Type, model
- серии Cardiolife модель TEC-7721K
- Manufacturer
- фирма Nihon Kohden Corporacion, Япония
- Certificate holder
- ТОО Medicus Eurasia, Казахстан, 050004, г. Алматы, ул. Желтоксана, 59, т/ф 500015, 509750, e-mail info@medicusEA.kz,
- Type approval certificate
- 4756
- Date of issue
- 02.09.2008
- Valid until
- 02.09.2013
- Verification interval
- 1 год
- Verification procedure
- МИ 1201-86 (Методические указания. ГСИ. Дефибрилляторы последовательного действия. 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.