KabiHelp® Uno - Indonesia BPOM Medical Device Registration
KabiHelp® Uno is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902420448. The device is manufactured by DIFFUPLAST SRL from Italy, 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
DIFFUPLAST SRLCountry of Origin
Italy
Authorized Representative
FRESENIUS KABI INDONESIAAR Address
Menara Bidakara 1 Lt 19, Jl. Jend Gatot Subroto Kav 71-73
Registration Date
May 07, 2024
Expiry Date
Feb 19, 2029
Product Type
Therapeutic General and Individual Hospital Equipment
I.V. container.
Non Electromedic Sterile
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