cobas SARS-CoV-2 & Influenza A/B Quality Control Kit for use on the cobas Liat Systems - Indonesia BPOM Medical Device Registration
cobas SARS-CoV-2 & Influenza A/B Quality Control Kit for use on the cobas Liat Systems is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101125398. The device is manufactured by ROCHE MOLECULAR SYSTEMS INC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ROCHE INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ROCHE MOLECULAR SYSTEMS INCCountry of Origin
United States
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
Jul 22, 2022
Expiry Date
Nov 19, 2025
Product Type
Clinical Chemistry Test System
Quality control material (assayed and unassayed) (cair)
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