MANI Swap Kit - Indonesia BPOM Medical Device Registration

MANI Swap Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203810821. The device is manufactured by MANI, INC., KIYOHARA FACTORY from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. OPHTHALINDO JAYA.

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