ROSSMAX Handheld Pulse Oximeter - Indonesia BPOM Medical Device Registration

ROSSMAX Handheld Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502818962. The device is manufactured by ROSSMAX INNOTEK from Taiwan (China), and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is 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.