Термометры медицинские ртутные максимальные стеклянные Biotherm® Clinical
Type approval of measuring instruments · reg. No. KZ.02.01.00591-2020
An expired certificate is not a ban. An instrument made in 2020–2025 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.02.01.00591-2020
- Name
- Термометры медицинские ртутные максимальные стеклянные
- Type, model
- Biotherm® Clinical
- Manufacturer
- фирма «Ningbo Greetmed Medical Instruments Co.",
- Certificate holder
- Товарищество с ограниченной ответственностью "Медицинская Фармацевтическая компания "БИОЛА\"", г. Алматы, ул. Бузурбаева 13, +7 (772) 738 23 06,E-mail:post@biola.kz
- Type approval certificate
- 591
- Date of issue
- 28.04.2020
- Valid until
- 28.04.2025
- Verification interval
- не подлежит периодической поверке
- Verification procedure
- KZ.04.02.04921-2010 «Термометры медицинские электронные цифровые Biotherm Budget модификации Digital, Flexible производства компании «Ningbo Greetmed Medical Instruments Co., Ltd», Китай. 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.