SEED 1dayPure Flex - Indonesia BPOM Medical Device Registration

SEED 1dayPure Flex is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21204026192. The device is manufactured by SEED CO., LTD from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. CREATIVE MANAGEMENT OPTICALS.

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