Murex HBsAg Version 3 - Indonesia BPOM Medical Device Registration

Murex HBsAg Version 3 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30305220498. The device is manufactured by DIASORIN ITALIA S.P.A UK BRANCH from United Kingdom, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. BIOMEDIKAL SCIENTIFIC INDONESIA.

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