Lenisna 200 - Indonesia BPOM Medical Device Registration

Lenisna 200 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602220116. The device is manufactured by SPIRIT CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PHARMINDO RHIZOME STURDY.

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