EIZO RadiForce RX850 - Indonesia BPOM Medical Device Registration

EIZO RadiForce RX850 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11501420306. The device is manufactured by EIZO CORPORATION from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. TRIPUTRA TECHNO MED.

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.