Certera

Cистемы ультразвуковые диагностические медицинские LOGIQ E9

Type approval of measuring instruments · reg. No. KZ.02.01.01617-2022

Type approved, certificate valid until 04.07.2027

Instruments of this type are listed in the GSI register of Kazakhstan and can be verified in Kazakhstan. Verification interval: 2 года.

Record data

Registration number
KZ.02.01.01617-2022
Name
Cистемы ультразвуковые диагностические медицинские
Type, model
LOGIQ E9
Manufacturer
фирма «GE Medical Systems Ultrasound & Primary care Diagnostics LLC (GE Healthcare)», США
Certificate holder
ТОО «Дженерал Электрик Казахстан», ,УЛИЦА ТИМИРЯЗЕВА, 28В, КВ ОФИС 307AdrAdrEng+7 (727) 232 11 20,
Type approval certificate
1617
Date of issue
04.07.2022
Valid until
04.07.2027
Verification interval
2 года
Verification procedure
KZ.04.02.06088-2011 «Система ультразвуковая диагностическая медицинская LOGIQ E9, производства «GE Medical Systems Ultrasound & Primary care Diagnostics LLC» (GE Healthcare) США, входящей в состав «GE Medical Systems Information Technologies Inc. США. 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.