3M ESPE KETAC Universal Aplicap - Indonesia BPOM Medical Device Registration

3M ESPE KETAC Universal Aplicap is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602420060. The device is manufactured by 3M DEUTSCHLAND GMBH., GERMANY from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is COBRA DENTAL INDONESIA.

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