ALIAXIN GP - Indonesia BPOM Medical Device Registration

ALIAXIN GP is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602320236. The device is manufactured by ROSE PHARMA SA from Switzerland, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. NEOASIA AESTHETIC INDONESIA.

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