BioR flex 01 BBS - Indonesia BPOM Medical Device Registration
BioR flex 01 BBS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209420214. 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 09, 2024
Expiry Date
Oct 25, 2029
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Empty container for the collection and processing of blood and blood components.
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