GSI Allegro - Indonesia BPOM Medical Device Registration

GSI Allegro is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20701914086. The device is manufactured by DGS DIAGNOSTICS SP. Z O.O from Poland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DEMKA SAKTI.

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