KOSEN PTFE Coated Guidewire - Indonesia BPOM Medical Device Registration

KOSEN PTFE Coated Guidewire is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805320868. The device is manufactured by TIANCK MEDICAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. LUCKY MEDICAL INDONESIA.

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