DIALIFE Fistula Needles - Indonesia BPOM Medical Device Registration

DIALIFE Fistula Needles is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805320617. The device is manufactured by DIALIFE SA from Switzerland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GRAHA KREASI MEDIKA.

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