OPTOMED Smartscope FA - Indonesia BPOM Medical Device Registration

OPTOMED Smartscope FA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201411710. The device is manufactured by OPTOMED LTD. from Finland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. EAST RAYA LESTARI.

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