The RED BiViDerma I - Indonesia BPOM Medical Device Registration

The RED BiViDerma I is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602420040. 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 MULTI-MILLION PARTNERS OF PERKASA INDONESIA.

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