COBAS CRP Test cobas b 101 - Indonesia BPOM Medical Device Registration
COBAS CRP Test cobas b 101 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305021712. The device is manufactured by PHC CORPORATION IN VITRO DIAGNOSTICS DIVISION from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ROCHE INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
PHC CORPORATION IN VITRO DIAGNOSTICS DIVISIONCountry of Origin
Japan
Authorized Representative
ROCHE INDONESIAAR Address
Gedung AIA Central Lantai 36 Jl. Jend. Sudirman KAV. 48A RT/RW 003/004 Kelurahan Karet Semanggi
Registration Date
Sep 03, 2024
Expiry Date
Jul 04, 2029
Product Type
Immunological Test System
C-reactive protein immunological test system.
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