JD BIOTECH Mycobacterium Tuberculosis Antigen Rapid Test Kit - Indonesia BPOM Medical Device Registration
JD BIOTECH Mycobacterium Tuberculosis Antigen Rapid Test Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303129432. The device is manufactured by JEI DANIEL (JD) BIOTECH CORP from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is Nelta Multi Gracia.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
JEI DANIEL (JD) BIOTECH CORPCountry of Origin
China
Authorized Representative
Nelta Multi GraciaAR Address
Metland Menteng. Jl. Menteng Niaga Blok J7 No.1 Ujung Menteng, Cakung, Jakarta Timur 13960
Registration Date
Jan 01, 2022
Expiry Date
Dec 31, 2023
Product Type
Serological Reagents
Mycobacterium tuberculosis immunofluorescent reagents.
Invitro Diagnostics
VIRCLIA AUXILIARY REAGENTS-EDB
VIRCELL S.L.
INVASIVE CANDIDIASIS (CAGTA) VIRCLIA IgG MONOTEST
VIRCELL S.L.
HELICOBACTER PYLORI Ag VIRCLIAยฎ MONOTEST
VIRCELL S.L
DIRECT SARS-COV-2 REAL TIME PCR KIT
VIRCELL SL
HELICOBACTER PYLORI VIRCLIAยฎ IgG MONOTEST
VIRCELL S.L
HERPES SIMPLEX 1+2 VIRCLIAยฎ IgG MONOTEST
VIRCELL S.L
HELICOBACTER PYLORI VIRCLIAยฎ IgA MONOTEST
VIRCELL S.L
SERION ELISA Control Helicobacter pylori IgG
INSTITUT VIRION\SERION GMBH
SERION ELISA Control Aspergillus fumigatus IgG
INSTITUT VIRION\SERION GMBH
MEASLES VIRCLIA IgM MONOTEST
VIRCELL S.L

