BIOBASE Capillary Centrifuge - Indonesia BPOM Medical Device Registration
BIOBASE Capillary Centrifuge is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10209420199. The device is manufactured by JINAN BIOBASE MEDICAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. PRIMASENTOSA CHRONICLE.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
JINAN BIOBASE MEDICAL CO., LTD.Country of Origin
China
Authorized Representative
PT. PRIMASENTOSA CHRONICLEAR Address
JL. RAYA JOGLO NO.19A JOGLO KEMBANGAN
Registration Date
May 29, 2024
Expiry Date
Oct 19, 2028
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Blood bank centrifuge for in vitro diagnostic use.
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