SEIMITSU Diluent - Indonesia BPOM Medical Device Registration

SEIMITSU Diluent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208918877. The device is manufactured by SHENZHEN HETO MEDICAL TECH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SEIMITSU DIAGNOSTICS.

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