LSSA - Indonesia BPOM Medical Device Registration

LSSA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603126738. The device is manufactured by NEWPONG CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. HAJU MEDICAL INDONESIA.

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