MANI® Dia-Burs - Indonesia BPOM Medical Device Registration

MANI® Dia-Burs is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10603420378. The device is manufactured by MANI HANOI CO., LTD. PHO YEN FACTORY from Vietnam, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MURSMEDIC.

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