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ROSSMAX Pulse Oximeter - Indonesia BPOM Medical Device Registration

ROSSMAX Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502213381. The device is manufactured by ROSSMAX INNOTEK CORP. from Taiwan (China), and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BRIDGE TWO.

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
ROSSMAX Pulse Oximeter
Analysis ID: AKL 20502213381

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Taiwan (China)

Authorized Representative

PT. BRIDGE TWO

AR Address

Jl. Petojo Melintang No. 17

Registration Date

Aug 08, 2024

Expiry Date

May 15, 2029

Product Type

Monitoring Cardiology Equipment

Oximeter.

Non Radiation Electromedics

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