NUGRA Hydrophilic Guide Wire - Indonesia BPOM Medical Device Registration

NUGRA Hydrophilic Guide Wire is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501420572. The device is manufactured by LEPU MEDICAL TECHNOLOGY (BEIJING) CO,. LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. NUGRA KARSERA.

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