TERUFUSION Administration Set for PUMP - Indonesia BPOM Medical Device Registration
TERUFUSION Administration Set for PUMP is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902020455. 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 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
TERUMO INDONESIAAR Address
Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta
Registration Date
Dec 04, 2023
Expiry Date
Oct 27, 2028
Product Type
Therapeutic General and Individual Hospital Equipment
Intravascular administration set
Non Electromedic Sterile
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