AT LARA 829MP - Indonesia BPOM Medical Device Registration

AT LARA 829MP is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31202320086. The device is manufactured by CARL ZEISS MEDITEC AG from Germany, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. CARL ZEISS NEW ZEISS.

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