TERUFUSION Blood Administration Set - Indonesia BPOM Medical Device Registration
TERUFUSION Blood Administration Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902803770. The device is manufactured by KOFU FACTORY OF TERUMO CORPORATION from Japan, 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
KOFU FACTORY OF TERUMO CORPORATIONCountry of Origin
Japan
Authorized Representative
PT. TERUMO INDONESIAAR Address
Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta
Registration Date
Mar 17, 2021
Expiry Date
Jan 15, 2026
Product Type
Therapeutic General and Individual Hospital Equipment
Intravascular administration set.
Non Electromedic Sterile
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