AIRMESO SCALP - Indonesia BPOM Medical Device Registration

AIRMESO SCALP is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902322038. The device is manufactured by MCURE., CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ETERNAL VAST OCEAN.

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