KENZA MAX Biochemistry Analyzer - Indonesia BPOM Medical Device Registration

KENZA MAX Biochemistry Analyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10102813470. The device is manufactured by BIOLABO, SA. from France, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. CIPTA VARIA KHARISMA UTAMA.

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