GENEWISE Fully-Automated Nucleic Acid Amplification Testing System - Indonesia BPOM Medical Device Registration

GENEWISE Fully-Automated Nucleic Acid Amplification Testing System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20304420035. The device is manufactured by GENEWISE BIO CO., LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is FOR ANY MEDICAL INDONESIA.

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