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ONECARE Pulse Oximeter - Indonesia BPOM Medical Device Registration

ONECARE Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502124543. The device is manufactured by SHENZHEN JUMPER MEDICAL EQUIPMENT CO, LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. CENTRAL MEDIKA INDONESIA.

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
ONECARE Pulse Oximeter
Analysis ID: AKL 20502124543

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. CENTRAL MEDIKA INDONESIA

AR Address

Jl. Candi Mutiara Selatan III/ 317 RT.03/06 Kalipancur

Registration Date

Jul 28, 2021

Expiry Date

Jul 28, 2024

Product Type

Monitoring Cardiology Equipment

Oximeter.

Non Radiation Electromedics

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