TERUFUSION Solution Administration Set for Infusion Pump - Indonesia BPOM Medical Device Registration
TERUFUSION Solution Administration Set for Infusion Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902220938. The device is manufactured by FORTE GROW MEDICAL (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
FORTE GROW MEDICAL (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
Aug 31, 2022
Expiry Date
Nov 12, 2025
Product Type
Therapeutic General and Individual Hospital Equipment
Intravascular administration set
Non Electromedic Sterile
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