VIRCELL TOXOPLASMA ELISA IgG - Indonesia BPOM Medical Device Registration
VIRCELL TOXOPLASMA ELISA IgG is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303321589. The device is manufactured by VIRCELL SL 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 SLCountry 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 05, 2023
Expiry Date
Dec 31, 2026
Product Type
Serological Reagents
Toxoplasma gondii serological reagents.
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VIRCELL ELISA SORBENT
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VIRCELL CYTOMEGALOVIRUS ELISA IgM CAPTURE
VIRCELL MEASLES ELISA IgG/IgM
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