COBAS SARS-CoV-2 Quality Control Kit for use on the cobas Liat System - Indonesia BPOM Medical Device Registration

COBAS SARS-CoV-2 Quality Control Kit for use on the cobas Liat System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101220306. The device is manufactured by ROCHE MOLECULAR SYSTEMS, INC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ROCHE INDONESIA.

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.