FRESENIUS KABI INJECTOMAT AGILIA Syringe Pump - Indonesia BPOM Medical Device Registration
FRESENIUS KABI INJECTOMAT AGILIA Syringe Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902701112. The device is manufactured by FRESENIUS VIAL. 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.Country of Origin
France
Authorized Representative
PT. FRESENIUS KABI INDONESIAAR Address
Menara Bidakara 1 Lt.19, Jl. Gatot Subroto Kav 71 - 73 Menteng Dalam, Tebet, Jakarta Selatan 12870
Registration Date
Apr 12, 2021
Expiry Date
Sep 10, 2024
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
Non Radiation Electromedics
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