FUSIOMED CRYOLIPOSCULPT - Indonesia BPOM Medical Device Registration

FUSIOMED CRYOLIPOSCULPT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603916106. The device is manufactured by BIOTEC ITALIA S.R.L from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is HERCA CIPTA DERMAL PERDANA.

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