RUMEX Vitreoretinal Set 23G - Indonesia BPOM Medical Device Registration

RUMEX Vitreoretinal Set 23G is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11203710645. The device is manufactured by RUMEX INSTRUMENTS LTD. from Russian Federation, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. PANCARAYA KRISNAMANDIRI.

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