DOPPLEX Ability - Indonesia BPOM Medical Device Registration

DOPPLEX Ability is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502028102. The device is manufactured by HUNTLEIGH HEALTHCARE LTD - DIAGNOSTIC PRODUCTS DIVISION from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. LABORA MANDIRI INDO PRATAMA.

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