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 20209914606. The device is manufactured by FRESENIUS HEMOCARE ITALIA S.R.L. from Italy, 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
FRESENIUS HEMOCARE ITALIA S.R.L.Country of Origin
Italy
Authorized Representative
PT. FRESENIUS KABI INDONESIAAR Address
Menara Bidakara 1 Lt 19, Jl. Jend Gatot Subroto Kav 71-73
Registration Date
Feb 02, 2024
Expiry Date
Mar 19, 2024
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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