BRM Digitalis - Indonesia BPOM Medical Device Registration

BRM Digitalis is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302420257. The device is manufactured by BRM EXTREMITIES S.R.L from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is EUFRAT WITH.

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