FUJIFILM SILVAMP Dengue NS1 Ag - Indonesia BPOM Medical Device Registration
FUJIFILM SILVAMP Dengue NS1 Ag is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303220680. The device is manufactured by FUJIFILM YUWA MEDICAL PRODUCTS VIETNAM COMPANY LIMITED from Vietnam, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is FUJIFILM INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
Vietnam
Authorized Representative
FUJIFILM INDONESIAAR Address
Eightyeight@Kasablanka Office Tower Lantai 36, Unit A, B dan C, Jl. Casablanca Kav. 88
Registration Date
Oct 05, 2022
Expiry Date
Jul 22, 2027
Product Type
Serological Reagents
Dengue virus serological reagents
Invitro Diagnostics
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