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 10204513083. The device is manufactured by TERUMO BCT INC. from United Kingdom, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. TERUMO INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
TERUMO BCT INC.Country of Origin
United Kingdom
Authorized Representative
PT. TERUMO INDONESIAAR Address
Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta
Registration Date
Dec 20, 2019
Expiry Date
Sep 24, 2024
Product Type
Reagents and Specimen Providers
General purpose reagent.
Invitro Diagnostics
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