KEWEI RV-IgM Test Kit - Indonesia BPOM Medical Device Registration

KEWEI RV-IgM Test Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303520053. The device is manufactured by BEIJING KEWEI CLINICAL DIAGNOSTIC REAGENT INC from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SUMIFIN CITRA ABADI.

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.