ARGUS LSM Patient Monitor - Indonesia BPOM Medical Device Registration

ARGUS LSM Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501111313. The device is manufactured by GUANGDONG BIOLIGHT MEDITECH, CO. LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is MULYA HUSADA JAYA.

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