Guideliner V3 Catheter - Indonesia BPOM Medical Device Registration

Guideliner V3 Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501420153. The device is manufactured by VASCULAR SOLUTIONS LLC from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is TELEFLEX MEDICAL INDONESIA.

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