WISONIC Patient Monitor - Indonesia BPOM Medical Device Registration

WISONIC Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502915646. The device is manufactured by SHENZHEN WISONIC MEDICAL TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. Tri Srikandi Jaya Indonesia.

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