C-Thru Hydrophilic Acrylic Foldable IOL - Indonesia BPOM Medical Device Registration

C-Thru Hydrophilic Acrylic Foldable IOL is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31202320161. The device is manufactured by OMNI LENS PVT., LTD. from India, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. VISIMED GLOBAL STANDALONE.

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.