RENACARE A.V Fistula Needle Set - Indonesia BPOM Medical Device Registration

RENACARE A.V Fistula Needle Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805220252. The device is manufactured by SUNDER BIOMEDICAL TECH., CO., LTD. from Taiwan (China), and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. RENALMED TIARA MAIN.

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