KDB Glide - Indonesia BPOM Medical Device Registration

KDB Glide is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11203420017. The device is manufactured by NEW WORLD MEDICAL, INC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PERFECT SINGLE OPTICS.

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