SIGVARIS Compreboot Standard - Indonesia BPOM Medical Device Registration

SIGVARIS Compreboot Standard is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11402022100. The device is manufactured by SIGVARIS AG from Switzerland, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. EURAMED MEDICAL INDONESIA.

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