PROTSMART ™ - Indonesia BPOM Medical Device Registration

PROTSMART ™ is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805420182. The device is manufactured by MEDICA S.P.A from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PRIMA CENTER MEDIKACITRA.

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