LIQUINOX ® - Indonesia BPOM Medical Device Registration

LIQUINOX ® is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903911670. The device is manufactured by ALCONOX, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. LABQUIP INDOPRIMA.

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