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RIESTER – Ri-fox N Pulse Oximeter - Indonesia BPOM Medical Device Registration

RIESTER – Ri-fox N Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502123454. 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 PT. LABORA MANDIRI INDO PRATAMA.

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
RIESTER – Ri-fox N Pulse Oximeter
Analysis ID: AKL 20502123454

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. LABORA MANDIRI INDO PRATAMA

AR Address

Jl. C. Simanjuntak No. 47

Registration Date

Jun 14, 2021

Expiry Date

Dec 31, 2025

Product Type

Monitoring Cardiology Equipment

Oximeter.

Non Radiation Electromedics

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