LUMIX PLUS - Indonesia BPOM Medical Device Registration

LUMIX PLUS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403220061. The device is manufactured by FISIOLINE S.R.L [REGISTER] from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is HARLISA TRUE AWARD.

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