OSTEOMED Kobygard System - Indonesia BPOM Medical Device Registration

OSTEOMED Kobygard System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303110657. The device is manufactured by OSTEOMED L.P. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. PRO-HEALTH INTERNATIONAL.

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