KabiHelp Duo - Indonesia BPOM Medical Device Registration
KabiHelp Duo is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902323093. The device is manufactured by DIFFUPLAST SRL from Italy, 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
DIFFUPLAST SRLCountry of Origin
Italy
Authorized Representative
PT. FRESENIUS KABI INDONESIAAR Address
Menara Bidakara 1 Lt 19, Jl. Jend Gatot Subroto Kav 71-73
Registration Date
Dec 29, 2023
Expiry Date
Jun 09, 2028
Product Type
Therapeutic General and Individual Hospital Equipment
I.V. container.
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