Plexa ProMRI S DX - Indonesia BPOM Medical Device Registration

Plexa ProMRI S DX is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503021828. The device is manufactured by BIOTRONIK SE & CO., KG from Germany, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is TRANSMEDIC INDONESIA.

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