MESOJET™ HY-PO RF M - Indonesia BPOM Medical Device Registration

MESOJET™ HY-PO RF M is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603323831. The device is manufactured by JEAN MARIE LORENZ S.R.L from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FIRST MEDIKACITRA CENTER.

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