LIFOTRONIC SARS-CoV-2 Nucleic Acid Detection Kit (Multiplex PCR Fluorescent Probe Method) - Indonesia BPOM Medical Device Registration
LIFOTRONIC SARS-CoV-2 Nucleic Acid Detection Kit (Multiplex PCR Fluorescent Probe Method) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303027495. The device is manufactured by SHENZHEN LIFOTRONIC TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is RAFA TOPAZ MAIN.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHENZHEN LIFOTRONIC TECHNOLOGY CO., LTD.Country of Origin
China
Authorized Representative
RAFA TOPAZ MAINAR Address
Taman Buaran Indah I Blok U No. 242 Jl. Radin Inten II, Klender, Jakarta Timur
Registration Date
Dec 11, 2021
Expiry Date
Dec 31, 2023
Product Type
Serological Reagents
Respiratory viral panel multiplex nucleic acid assay
Invitro Diagnostics
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