Certera

Монитор пациента IntelliVue MP (M8105A)

Type approval of measuring instruments · reg. No. KZ.02.02.03002-2012

Archived record: the certificate was valid 2012–2017

An expired certificate is not a ban. An instrument made in 2012–2017 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.02.02.03002-2012
Name
Монитор пациента
Type, model
IntelliVue MP (M8105A)
Manufacturer
фирма Philips Medizin Systeme Boblingen GmbH, Германия
Certificate holder
ТОО , г. Алматы, пр. Райымбека,/ул. Коммунальная, 169/1, т +7 (727) 250 71 94,
Type approval certificate
8451
Date of issue
10.07.2012
Valid until
10.07.2017
Verification interval
2 года

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.