INDO REAGEN Chemistry Control Level 2 Human Serum Based (Lyophilized) - Indonesia BPOM Medical Device Registration

INDO REAGEN Chemistry Control Level 2 Human Serum Based (Lyophilized) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101020612. The device is manufactured by HORIBA INSTRUMEN INCORPORATION from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SEGARA HUSADA MANDIRI.

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.