Bluephase® N G4 - Indonesia BPOM Medical Device Registration

Bluephase® N G4 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20605320949. The device is manufactured by IVOCLAR VIVADENT MANUFACTURING GMBH from Austria, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MURSMEDIC.

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