TRUSCAN PRO - Indonesia BPOM Medical Device Registration

TRUSCAN PRO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203026604. The device is manufactured by LIGHTMED USA, INC from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TRIUMPHANT MANDARIN OPTO-MEDIC.

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