KEELER Prismatic Loupes - Indonesia BPOM Medical Device Registration

KEELER Prismatic Loupes is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11203719310. The device is manufactured by KEELER LIMITED. from United Kingdom, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. FADZKURUNI.

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