GENBODY COVID-19 Ag - Indonesia BPOM Medical Device Registration

GENBODY COVID-19 Ag is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303024756. The device is manufactured by GENBODY INC. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GENBODY INDONESIA SEJAHTERA.

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