BioP flex BS PF - Indonesia BPOM Medical Device Registration
BioP flex BS PF is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902420533. The device is manufactured by FENWAL INTERNATIONAL, INC. from Dominican, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FRESENIUS KABI INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FENWAL INTERNATIONAL, INC.Country of Origin
Dominican
Authorized Representative
PT. FRESENIUS KABI INDONESIAAR Address
Menara Bidakara 1 Lt 19, Jl. Jend Gatot Subroto Kav 71-73
Registration Date
Jun 04, 2024
Expiry Date
Oct 25, 2028
Product Type
Therapeutic General and Individual Hospital Equipment
Intravascular administration set
Non Electromedic Sterile
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