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 31002320192. The device is manufactured by MICROVENTION EUROPE from France, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is ADMIRAL BLESENSA IMMORTAL.

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