ET III SA Fixture System - Indonesia BPOM Medical Device Registration

ET III SA Fixture System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602710586. The device is manufactured by HIOSSEN INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. OSSTEM IMPLANT.

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.