ZEISS Clarus 500 - Indonesia BPOM Medical Device Registration

ZEISS Clarus 500 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201124192. The device is manufactured by CARL ZEISS MEDITEC INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ELO KARSA UTAMA.

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