TIANLONG Influenza A/Influenza B/SARS-CoV-2 Nucleic Acid Detection Kit (Fluorescence PCR Method) - Indonesia BPOM Medical Device Registration
TIANLONG Influenza A/Influenza B/SARS-CoV-2 Nucleic Acid Detection Kit (Fluorescence PCR Method) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303420644. The device is manufactured by SUZHOU TIANLONG BIOTECHNOLOGY, CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is INTERSKALA MEDIKA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SUZHOU TIANLONG BIOTECHNOLOGY, CO., LTDCountry of Origin
China
Authorized Representative
INTERSKALA MEDIKA INDONESIAAR Address
Green Sedayu Biz Park Blok DM 9/62, Jalan Daan Mogot Km.18
Registration Date
Dec 06, 2024
Expiry Date
Sep 05, 2027
Product Type
Serological Reagents
Respiratory viral panel multiplex nucleic acid assay
Invitro Diagnostics
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