VENOSAN 4000 - Indonesia BPOM Medical Device Registration

VENOSAN 4000 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10902322104. The device is manufactured by SWISSLASTICS BY from Switzerland, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. INDOMED KAHANASTI INDONESIA.

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