GSI 39 Auto Tymp - Indonesia BPOM Medical Device Registration

GSI 39 Auto Tymp is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20701812226. 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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