Системы мониторинга пациента MAGLIFE, модификаций Serenity, Light
Type approval of measuring instruments · reg. No. KZ.02.01.01485-2022
Instruments of this type are listed in the GSI register of Kazakhstan and can be verified in Kazakhstan. Verification interval: 1 год.
Record data
- Registration number
- KZ.02.01.01485-2022
- Name
- Системы мониторинга пациента
- Type, model
- MAGLIFE, модификаций Serenity, Light
- Manufacturer
- фирма «Schiller AG»,«Schiller AG» фирмасы,040,04000,04000000,Altgasse 68, 6341 Baar,-,AdrAdrEng
- Certificate holder
- ТОО «НаноФарм», 050060, г. Алматы, Бостандыкский р-н, ул. Экспериментальная база, 3а,НаноФарм ЖШС, 050060, Алматы қ., Бостандық ауд., эксперименталдық база к-сі, 3а,118,11816,11816206,050060, г. Алматы, Бостандыкский р-н, ул. Экспериментальная база, 3а,Алматы қаласы, Экспериментальная база, 3 а көшесі,AdrAdrEng+7 (727) 393 68 34,Emailinfo@nanopharm.kz,
- Type approval certificate
- 1485
- Date of issue
- 05.04.2022
- Valid until
- 05.04.2027
- Verification interval
- 1 год
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.