ARIA H. Pylori Ab Combo Rapid Test - Indonesia BPOM Medical Device Registration

ARIA H. Pylori Ab Combo Rapid Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303321367. The device is manufactured by BEIJING GENESEE BIOTECH, INC. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is HERMAN MEDTEK DIAGNOSTICS.

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