TERUFLEX CPDA-1 Single Blood Bag - Indonesia BPOM Medical Device Registration
TERUFLEX CPDA-1 Single Blood Bag is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209711297. The device is manufactured by TERUMO BCT VIETNAM CO., LTD. from Vietnam, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TERUMO INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TERUMO BCT VIETNAM CO., LTD.Country of Origin
Vietnam
Authorized Representative
PT. TERUMO INDONESIAAR Address
Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta
Registration Date
Apr 07, 2021
Expiry Date
Mar 08, 2026
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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