AiBS-01 - Indonesia BPOM Medical Device Registration

AiBS-01 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501420486. The device is manufactured by FUTURE INC. from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is QUALTEK CONSULTANT JAKARTA.

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