FRESENIUS KABI Infusia Syringe Pump SP7 - Indonesia BPOM Medical Device Registration
FRESENIUS KABI Infusia Syringe Pump SP7 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902021177. 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 PT. FRESENIUS KABI INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FRESENIUS KABI (NANCHANG) CO.,LTDCountry of Origin
China
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
Mar 17, 2020
Expiry Date
Jan 06, 2025
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
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