ZEISS OPMI Lumera 300 - Indonesia BPOM Medical Device Registration

ZEISS OPMI Lumera 300 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603421708. The device is manufactured by CARL ZEISS SUZHOU CO., LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is CARL ZEISS NEW ZEISS.

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