ZEISS IOLMaster 500 - Indonesia BPOM Medical Device Registration

ZEISS IOLMaster 500 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201420191. The device is manufactured by CARL ZEISS MEDITEC AG from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is CARL ZEISS NEW ZEISS.

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