AT TORBI 709 - Indonesia BPOM Medical Device Registration

AT TORBI 709 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31202520008. The device is manufactured by CARL ZEISS MEDITEC SAS from France, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. CARL ZEISS NEW ZEISS.

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