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MICROLIFE Finger pulse oximeter - Indonesia BPOM Medical Device Registration

MICROLIFE Finger pulse oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502320901. The device is manufactured by BEIJING CHOICE ELECTRONIC TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is CEKINDO BUSINESS INTERNATIONAL.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
MICROLIFE Finger pulse oximeter
Analysis ID: AKL 20502320901

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

CEKINDO BUSINESS INTERNATIONAL

AR Address

CEKINDO BUSINESS INTERNATIONAL

Registration Date

Nov 17, 2023

Expiry Date

Aug 28, 2028

Product Type

Monitoring Cardiology Equipment

Oximeter.

Non Radiation Electromedics

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