DIROS RF CANNULA - Indonesia BPOM Medical Device Registration

DIROS RF CANNULA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21002812502. The device is manufactured by DIROS TECHNOLOGY INC from Canada, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SCHMIDT BIOMEDTECH INDONESIA.

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