TERUFUSION Syringe Pump - Indonesia BPOM Medical Device Registration
TERUFUSION Syringe Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902719347. The device is manufactured by ASHITAKA FACTORY OF TERUMO CORPORATION JAPAN from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TERUMO INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ASHITAKA FACTORY OF TERUMO CORPORATION JAPANCountry of Origin
Japan
Authorized Representative
PT. TERUMO INDONESIAAR Address
Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta
Registration Date
Aug 11, 2022
Expiry Date
May 24, 2027
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
Non Radiation Electromedics
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