TERUMO Platelet Additive Solution + (T-PAS+) - Indonesia BPOM Medical Device Registration
TERUMO Platelet Additive Solution + (T-PAS+) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209320782. The device is manufactured by TERUMO BCT., LTD. from United Kingdom, 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., LTD.Country of Origin
United Kingdom
Authorized Representative
PT. TERUMO INDONESIAAR Address
Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta
Registration Date
Dec 14, 2023
Expiry Date
Oct 04, 2027
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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