GENOSS OSTEON II Synthetic Bone Graft Substitute - Indonesia BPOM Medical Device Registration

GENOSS OSTEON II Synthetic Bone Graft Substitute is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602817312. The device is manufactured by COMRADE CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ICT WORLDWIDE INDONESIA.

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