SENDOLINE Peeso Reamer - Indonesia BPOM Medical Device Registration

SENDOLINE Peeso Reamer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10603718016. The device is manufactured by SENDOLINE AB from Sweden, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. COBRA DENTAL INDONESIA.

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