FRESENIUS AMIKA Infusion Pump - Indonesia BPOM Medical Device Registration
FRESENIUS AMIKA Infusion Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902512824. The device is manufactured by FRESENIUS VIAL S.A.S. from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FRESENIUS KABI INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FRESENIUS VIAL S.A.S.Country of Origin
France
Authorized Representative
PT. FRESENIUS KABI INDONESIAAR Address
Menara Bidakara 1 Lt 19, Jl. Jend Gatot Subroto Kav 71-73
Registration Date
Jan 05, 2024
Expiry Date
Oct 19, 2028
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
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