MKCELLS Hollow Fiber Hemodiafilter - Indonesia BPOM Medical Device Registration

MKCELLS Hollow Fiber Hemodiafilter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805320710. The device is manufactured by CHENGDU OCI MEDICAL DEVICES CO., LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. INTERSKALA SEHAT SEJAHTERA.

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