CALIBRA Veneer - Indonesia BPOM Medical Device Registration

CALIBRA Veneer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602220200. The device is manufactured by DENTSPLY CAULK from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is DENTSPLY SIRONA INDONESIA.

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