TERUFUSION Solution Administration Set - Indonesia BPOM Medical Device Registration
TERUFUSION Solution Administration Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902817789. The device is manufactured by PERFECT MEDICAL INDUSTRY (VN) CO., LTD. from Vietnam, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is TERUMO INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
PERFECT MEDICAL INDUSTRY (VN) CO., LTD.Country of Origin
Vietnam
Authorized Representative
TERUMO INDONESIAAR Address
Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta
Registration Date
Apr 03, 2023
Expiry Date
Feb 02, 2028
Product Type
Therapeutic General and Individual Hospital Equipment
Intravascular administration set
Non Electromedic Sterile
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