COMPOFLEX 3F 63 ml CPDA-1 PDS-V - Indonesia BPOM Medical Device Registration
COMPOFLEX 3F 63 ml CPDA-1 PDS-V is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209807752. The device is manufactured by FRESENIUS KABI (GUANGZHOU) CO., LTD. from China, 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 (GUANGZHOU) CO., LTD.Country of Origin
China
Authorized Representative
PT. FRESENIUS KABI INDONESIAAR Address
Menara Bidakara 1 Lt 19, Jl. Jend Gatot Subroto Kav 71-73
Registration Date
Nov 25, 2024
Expiry Date
Sep 05, 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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