PHILIPS O3 Module - Indonesia BPOM Medical Device Registration

PHILIPS O3 Module is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502024803. The device is manufactured by PHILIPS MEDIZIN SYSTEME BOEBLINGEN GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PHILIPS INDONESIA COMMERCIAL.

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