Амбулаторные регистраторы ЭКГ по Холтеру CardioMera
Type approval of measuring instruments · reg. No. KZ.02.01.01033-2021
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.02.01.01033-2021
- Name
- Амбулаторные регистраторы ЭКГ по Холтеру
- Type, model
- CardioMera
- Manufacturer
- фирма Meditech Ltd., Венгрия
- Certificate holder
- 060440004007,Акционерное общество Ordamed, г. Алматы, ул. Курмангазы, 141, п. 3Казахстан, г. Алматы, ул. Курмангазы, 141, п. 3+7 (727) 270 70 72,Emailinfo@ordamed.kz,
- Type approval certificate
- 1033
- Date of issue
- 27.05.2021
- Valid until
- 27.05.2026
- Verification interval
- 1 год
- Verification procedure
- KZ.04.02.10368-2016 "Амбулаторные регистраторы ЭКГ по Холтеру CardioMera, производства фирмы "Meditech Ltd.", Венгрия. 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.