TERUFUSION™ SS 10 - Indonesia BPOM Medical Device Registration
TERUFUSION™ SS 10 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902421143. The device is manufactured by SANMINA-SCI (SHENZHEN) LTD. from China, 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
SANMINA-SCI (SHENZHEN) LTD.Country of Origin
China
Authorized Representative
TERUMO INDONESIAAR Address
Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta
Registration Date
Oct 03, 2024
Expiry Date
Jun 20, 2029
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
Non Radiation Electromedics
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