YHLO iFlash-EB VCA IgA - Indonesia BPOM Medical Device Registration
YHLO iFlash-EB VCA IgA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303220800. The device is manufactured by SHENZHEN YHLO BIOTECH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FAITHFUL MEDICAL GRACE.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHENZHEN YHLO BIOTECH CO., LTD.Country of Origin
China
Authorized Representative
PT. FAITHFUL MEDICAL GRACEAR Address
Mitra Sunter Boulevard Blok B No.39 Jl. Yos Sudarso Kav. 89
Registration Date
Nov 16, 2022
Expiry Date
Feb 04, 2026
Product Type
Serological Reagents
Epstein-Barr virus serological reagents.
Invitro Diagnostics
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YHLO UNICELL-AMH
YHLO UNICELL-PCT
YHLO UNICELL-S Immunofluorescence Reader dan Accessories
YHLO iFlash-Mycoplasma pn. IgM
YHLO iFlash-Chlamydia pn. IgM
YHLO iFlash-Chlamydia pn. IgG
YHLO iFlash-EB NA IgA
YHLO Rubella IgM Control
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