LumiraDx CRP Test - Indonesia BPOM Medical Device Registration

LumiraDx CRP Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305420241. The device is manufactured by LUMIRADX UK, LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDQUEST GLOBAL PARTNERS.

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