SCHEBO Master Quick-Prep™ - Indonesia BPOM Medical Device Registration

SCHEBO Master Quick-Prep™ is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10203420187. The device is manufactured by SCHEBO BIOTECH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. FRIMUST ADIJAYA UTAMA.

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