LVIS Intraluminal Support Device - Indonesia BPOM Medical Device Registration

LVIS Intraluminal Support Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31002915042. The device is manufactured by MICROVENTION, INC. from United States, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. ADMIRAL BLESENSA IMMORTAL.

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