COBAS ISE Diluent Gen.2 cobas c systems - Indonesia BPOM Medical Device Registration
COBAS ISE Diluent Gen.2 cobas c systems is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101111917. The device is manufactured by ROCHE DIAGNOSTICS GMBH. from Germany, 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 DIAGNOSTICS GMBH.Country 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
Dec 17, 2024
Expiry Date
Aug 22, 2029
Product Type
Clinical Chemistry Test System
Sodium test system (kit & cair)
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