COBAS S1 Rinse Solution cobas b 221, Roche OMNI S - Indonesia BPOM Medical Device Registration
COBAS S1 Rinse Solution cobas b 221, Roche OMNI S is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204611165. The device is manufactured by ROCHE DIAGNOSTICS INTL, LTD. from Switzerland, 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 INTL, LTD.Country of Origin
Switzerland
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
Oct 07, 2024
Expiry Date
Jul 04, 2029
Product Type
Reagents and Specimen Providers
General purpose reagent.
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