'PURIBLOOD" Leukocyte reduction filter for red blood cells - Indonesia BPOM Medical Device Registration
'PURIBLOOD" Leukocyte reduction filter for red blood cells is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209028127. The device is manufactured by INNOVATIVE MEDICAL MANUFACTURING COMPANY from Taiwan (China), and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is QUALTEK CONSULTANT JAKARTA.
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โPURIBLOODโ Leukocyte reduction filter for red blood cells
Risk Classification
Product Class
Kelas : 2
Manufacturer
INNOVATIVE MEDICAL MANUFACTURING COMPANYCountry of Origin
Taiwan (China)
Authorized Representative
QUALTEK CONSULTANT JAKARTAAR Address
Icon Business Park Blok K No 6, BSD City, Kab Tangerang, Banten
Registration Date
Dec 22, 2020
Expiry Date
Oct 30, 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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