Q-MAY Multiple Sera A Type K - Indonesia BPOM Medical Device Registration

Q-MAY Multiple Sera A Type K is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208110807. The device is manufactured by Q-MAY LABORATORY CORPORATION from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SUMBERMITRA AGUNGJAYA.

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