SIEMENS Sensis Vibe - Indonesia BPOM Medical Device Registration

SIEMENS Sensis Vibe is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501123087. The device is manufactured by SIEMENS HEALTHINEERS AG, ADVANCED THERAPIES from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SIEMENS HEALTHINEERS INDONESIA.

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