LUMIGLAM S - Indonesia BPOM Medical Device Registration

LUMIGLAM S is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602420077. The device is manufactured by BIOPLUS CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. SOMETECH NEW Zealand.

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