ZEISS KINEVO 900 - Indonesia BPOM Medical Device Registration

ZEISS KINEVO 900 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603520039. 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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