COCHLEAR NUCLEUS CI500 Series Non-Sterile Silicone Implant Template - Indonesia BPOM Medical Device Registration

COCHLEAR NUCLEUS CI500 Series Non-Sterile Silicone Implant Template is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30703023029. The device is manufactured by COCHLEAR LTD. from Australia, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. KASOEM HEARING.

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.