ZEISS OPMI Lumera 700 - Indonesia BPOM Medical Device Registration

ZEISS OPMI Lumera 700 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603421576. The device is manufactured by CARL ZEISS MEDITEC AG from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. CARL ZEISS NEW ZEISS.

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