Certera

Мониторы пациента варианты исполнения B105P, B125P, B105M, B125M, B155M.

Type approval of measuring instruments · reg. No. KZ.02.01.01761-2022

Type approved, certificate valid until 29.09.2027

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.02.01.01761-2022
Name
Мониторы пациента
Type, model
варианты исполнения B105P, B125P, B105M, B125M, B155M.
Manufacturer
фирма «GE Medical Systems Information Technologies, Inc.» США, на производственной площадке «GE Medical Systems (China) Co., Ltd.» Китай.,АҚШ, GE Medical Systems Information Technologies, Inc. фирмасы өндіріс алаңында Қытай, GE Medical Systems (China) Co., Ltd..,223,22300,22300000,-AdrAdrEng
Certificate holder
ТОО «Медико-Инновационные Технологии».,Медициналық-Инновациялық Технологиялар ЖШС.,118,11816,11816201,ул. Наурызбай батыра, 17, офис 311AdrAdrEng+7 (727) 258 17 45,
Type approval certificate
1761
Date of issue
29.09.2022
Valid until
29.09.2027
Verification interval
1 год

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 27.09.2026. The information is for reference — always confirm against the register and the instrument documents.