MIFILL Deep Lidocaine - Indonesia BPOM Medical Device Registration

MIFILL Deep Lidocaine is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602220037. 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 HERCA CIPTA DERMAL PERDANA.

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