ICONTROL CPDA-1 Triple Blood Bag - Indonesia BPOM Medical Device Registration
ICONTROL CPDA-1 Triple Blood Bag is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209220054. The device is manufactured by JIAXING TIANHE PHARMACEUTICAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MITRA BAHAGIA CITRA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
JIAXING TIANHE PHARMACEUTICAL CO., LTD.Country of Origin
China
Authorized Representative
PT. MITRA BAHAGIA CITRA MEDIKAAR Address
Jl. Raya Kalirungkut 27 Blok C-63
Registration Date
Mar 25, 2022
Expiry Date
Dec 15, 2025
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Empty container for the collection and processing of blood and blood components.
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