XELA REDERM 1,1% - Indonesia BPOM Medical Device Registration

XELA REDERM 1,1% is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602916035. The device is manufactured by DIACO BIOFARMACEUTICI S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. UNISON MEDIKA JAYA.

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