COBAS p 671 Centrifuge Unit - Indonesia BPOM Medical Device Registration
COBAS p 671 Centrifuge Unit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10209420209. The device is manufactured by ROCHE DIAGNOSTICS AUTOMATION SOLUTIONS GMBH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ROCHE INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
ROCHE DIAGNOSTICS AUTOMATION SOLUTIONS GMBHCountry of Origin
Germany
Authorized Representative
PT. ROCHE INDONESIAAR Address
Gedung AIA Central Lantai 36 Jl. Jend. Sudirman KAV. 48A RT/RW 003/004 Kelurahan Karet Semanggi
Registration Date
Jun 03, 2024
Expiry Date
Mar 20, 2029
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Blood bank centrifuge for in vitro diagnostic use.
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