AMO iDesign Refractive Studio System - Indonesia BPOM Medical Device Registration

AMO iDesign Refractive Studio System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201025096. The device is manufactured by AMO MANUFACTURING USA, LLC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MEDIUM FIRST.

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.