DENGUE VIRCLIA IgM MONOTEST - Indonesia BPOM Medical Device Registration
DENGUE VIRCLIA IgM MONOTEST is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303420188. The device is manufactured by VIRCELL S.L from Spain, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. NELTA MULTI GRACIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
VIRCELL S.LCountry of Origin
Spain
Authorized Representative
PT. NELTA MULTI GRACIAAR Address
Metland Menteng. Jl. Menteng Niaga Blok J7 No.1 Ujung Menteng, Cakung, Jakarta Timur 13960
Registration Date
May 15, 2024
Expiry Date
Dec 31, 2026
Product Type
Serological Reagents
Dengue virus serological reagents
Invitro Diagnostics
VIRCLIA AUXILIARY REAGENTS-EDP
VIRCLIA Auxiliary Reagents
HELICOBACTER PYLORI Ag VIRCLIA® MONOTEST
VIRCLIA AUXILIARY REAGENTS-DS
HELICOBACTER PYLORI VIRCLIA® IgG MONOTEST
HELICOBACTER PYLORI VIRCLIA® IgA MONOTEST
HERPES SIMPLEX 1+2 VIRCLIA® IgG MONOTEST
ASPERGILLUS GALACTOMANNAN AG VIRCLIA MONOTEST
MEASLES VIRCLIA IgM MONOTEST
RUBELLA VIRCLIA IgG MONOTEST
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