K1MED Magsclupt Electomagnetic Therapy Stimulator - Indonesia BPOM Medical Device Registration

K1MED Magsclupt Electomagnetic Therapy Stimulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403220060. The device is manufactured by K1MED CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BCS PRIMA INDONESIA.

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