Vision DX 41 - Indonesia BPOM Medical Device Registration

Vision DX 41 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10203122732. The device is manufactured by VISION ENGINEERING, LTD from United Kingdom, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is MULTISERA INDOSA.

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