Us2.v1 - Indonesia BPOM Medical Device Registration

Us2.v1 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501220482. The device is manufactured by EKO. AI PTE. LTD. from Singapore, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. QUALTEK CONSULTANT JAKARTA.

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