BioR flex 01 BBS PAEDI - Indonesia BPOM Medical Device Registration
BioR flex 01 BBS PAEDI is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209420178. 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 FRESENIUS KABI INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FENWAL INTERNATIONAL, INC.Country of Origin
Dominican
Authorized Representative
FRESENIUS KABI INDONESIAAR Address
Menara Bidakara 1 Lt 19, Jl. Jend Gatot Subroto Kav 71-73
Registration Date
May 16, 2024
Expiry Date
Oct 25, 2028
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.
Non Electromedic Sterile
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