TUOREN Reinforced Endotracheal Tube - Indonesia BPOM Medical Device Registration

TUOREN Reinforced Endotracheal Tube is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403120855. The device is manufactured by HENAN TUOREN MEDICAL DEVICE CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SINAR PANCA MEDIKA.

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