DR DIAGNOSTIC FE Focus B II - Indonesia BPOM Medical Device Registration
DR DIAGNOSTIC FE Focus B II is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204125064. The device is manufactured by DIRUI INDUSTRIAL CO., LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. GOLDEN MEDIKA MANDIRI.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
DIRUI INDUSTRIAL CO., LTDCountry of Origin
China
Authorized Representative
PT. GOLDEN MEDIKA MANDIRIAR Address
Jl. Raya Kalirungkut 27 Blok C-65
Registration Date
Aug 19, 2021
Expiry Date
Feb 14, 2024
Product Type
Reagents and Specimen Providers
General purpose reagent.
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