COMPOSTOP Flex T&B - Indonesia BPOM Medical Device Registration
COMPOSTOP Flex T&B is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209613897. The device is manufactured by FRESENIUS KABI HORATEV CZ S.R.O. from Czech Republic, 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 KABI HORATEV CZ S.R.O.Country of Origin
Czech Republic
Authorized Representative
PT. FRESENIUS KABI INDONESIAAR Address
Menara Bidakara 1 Lt.19, Jl. Gatot Subroto Kav 71 - 73 Menteng Dalam, Tebet, Jakarta Selatan 12870
Registration Date
Feb 20, 2023
Expiry Date
Sep 10, 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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