KERR OPTIBOND UNIVERSAL - Indonesia BPOM Medical Device Registration

KERR OPTIBOND UNIVERSAL is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602420361. The device is manufactured by KERR CORPORATION from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is TIGASATU MEDIKA SOLUSINDO.

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