Amika INT - Indonesia BPOM Medical Device Registration
Amika INT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902321948. The device is manufactured by FRESENIUS KABI NANCHANG CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is FRESENIUS KABI INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FRESENIUS KABI NANCHANG CO., LTD.Country of Origin
China
Authorized Representative
FRESENIUS KABI INDONESIAAR Address
Menara Bidakara 1 Lt.19, Jl. Gatot Subroto Kav 71 - 73 Menteng Dalam, Tebet, Jakarta Selatan 12870
Registration Date
Apr 18, 2023
Expiry Date
Sep 09, 2027
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
Non Radiation Electromedics
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