ZEESAN MDR-TB Test Kit (MMCA) - Indonesia BPOM Medical Device Registration

ZEESAN MDR-TB Test Kit (MMCA) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303321217. The device is manufactured by XIAMEN ZEESAN BIOTECH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SYNERGY INDOMITRA PRATAMA.

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