TERUFUSION Infusion Pump Type LM3 - Indonesia BPOM Medical Device Registration
TERUFUSION Infusion Pump Type LM3 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902814287. The device is manufactured by ASHITAKA FACTORY OF TERUMO CORPORATION. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is TERUMO INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ASHITAKA FACTORY OF TERUMO CORPORATION.Country of Origin
Japan
Authorized Representative
TERUMO INDONESIAAR Address
Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta
Registration Date
Feb 09, 2023
Expiry Date
Sep 15, 2027
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
Non Radiation Electromedics
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