AGAPPE DX3 Diluent - Indonesia BPOM Medical Device Registration

AGAPPE DX3 Diluent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208220145. The device is manufactured by AGAPPE DIAGNOSTICS LTD from India, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PHILIA CREATE HARMONY.

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