VISIOSTAR Ureteral Stent Kit - Indonesia BPOM Medical Device Registration

VISIOSTAR Ureteral Stent Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20804810115. The device is manufactured by UROVISION GESELLSCHAFT FÜR MEDIZINISCHE TECHNOLOGIE-TRANSFER MBH. from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SINAR MULIA INDOMEDIKA.

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.