PHILIPS Invivo Cannula - Indonesia BPOM Medical Device Registration

PHILIPS Invivo Cannula is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20401420040. The device is manufactured by SALTER LABS DE MEXICO S.A DE C.V. from Mexico, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PHILIPS INDONESIA COMMERCIAL.

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