VENTANA DP 200 and Accessories - Indonesia BPOM Medical Device Registration
VENTANA DP 200 and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20203918285. The device is manufactured by FFEI LTD. from United Kingdom, 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
FFEI LTD.Country of Origin
United Kingdom
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
Mar 22, 2024
Expiry Date
Oct 05, 2028
Product Type
Pathology Equipment and Accessories
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