VENTANA OptiView Amplification Kit - Indonesia BPOM Medical Device Registration
VENTANA OptiView Amplification Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10201410684. The device is manufactured by VENTANA MEDICAL SYSTEMS INC. from United States, 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
VENTANA MEDICAL SYSTEMS INC.Country 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
Feb 26, 2023
Expiry Date
Dec 19, 2027
Product Type
Biological Dyes
Dye and chemical solution stains.
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