AGNES - Indonesia BPOM Medical Device Registration

AGNES is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603325167. The device is manufactured by AGNES MEDICAL CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is SMELL MEDICAL INDONESIA.

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