DRYMAX Triple - Indonesia BPOM Medical Device Registration

DRYMAX Triple is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10903613313. The device is manufactured by ABSORBEST AB. from Sweden, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. EUPHRATES WITH.

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