KLFMED Infusion Set For Single Use - Indonesia BPOM Medical Device Registration

KLFMED Infusion Set For Single Use is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902810135. The device is manufactured by WENZHOU K.L.F. MEDICAL PLASTICS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEDICAL GREY INTERNATIONAL.

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