SEJONG LAPORT-CS - Indonesia BPOM Medical Device Registration

SEJONG LAPORT-CS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801815400. The device is manufactured by SEJONG MEDICAL CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SOMETECH NEW Zealand.

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