iFuge C4000 NXT - Indonesia BPOM Medical Device Registration
iFuge C4000 NXT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209420454. The device is manufactured by ACCUMAX LAB DEVICES PVT. LTD. from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. REDO MARKETING INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ACCUMAX LAB DEVICES PVT. LTD.Country of Origin
India
Authorized Representative
PT. REDO MARKETING INDONESIAAR Address
Ruko Renata Jl.Jalur Sutera Timur Blok 1A No. 9 Alam Sutera Kel. Kunciran Kec. Pinang
Registration Date
Nov 26, 2024
Expiry Date
Sep 02, 2029
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Automated cell-washing centrifuge for immuno-hematology.
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