KLS Martin Bos System - Indonesia BPOM Medical Device Registration

KLS Martin Bos System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603422421. The device is manufactured by KLS MARTIN SE & CO. KG from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. IMEDITECH SOLUTIONS INDONESIA.

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