VISUPLAN 500 - Indonesia BPOM Medical Device Registration

VISUPLAN 500 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201220120. The device is manufactured by REICHERT INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is CARL ZEISS NEW ZEISS.

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