CHRISTIE VeinViewer 3.0 Flex - Indonesia BPOM Medical Device Registration
CHRISTIE VeinViewer 3.0 Flex is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10903021863. The device is manufactured by MINNETRONIX INC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. IDS MEDICAL SYSTEMS INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
MINNETRONIX INC.Country of Origin
United States
Authorized Representative
PT. IDS MEDICAL SYSTEMS INDONESIAAR Address
Gedung Wisma 76, Lantai 17 & 22, Jl. LetJend. S. Parman Kav.76, Kelurahan Slipi, Kecamatan Palmerah, 11410
Registration Date
Jun 09, 2024
Expiry Date
Jan 16, 2028
Product Type
General Hospital Equipment and Other Individuals
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