VIRCLIA Extraction Tube - Indonesia BPOM Medical Device Registration
VIRCLIA Extraction Tube is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204420303. The device is manufactured by VIRCELL S.L. from Spain, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. NELTA MULTI GRACIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
VIRCELL S.L.Country 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
Dec 13, 2024
Expiry Date
Dec 31, 2026
Product Type
Reagents and Specimen Providers
General purpose reagent.
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