TIANLONG Novel Coronavirus (2019-nCoV) Nucleic Acid Detection Kit (Fluorescence PCR Method) - Indonesia BPOM Medical Device Registration
TIANLONG Novel Coronavirus (2019-nCoV) 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 20303027917. 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 PT. INTERSKALA MEDIKA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SUZHOU TIANLONG BIOTECHNOLOGY CO., LTD.Country of Origin
China
Authorized Representative
PT. INTERSKALA MEDIKA INDONESIAAR Address
Green Sedayu Biz Park Blok DM 9/62, Jalan Daan Mogot Km.18
Registration Date
Nov 23, 2023
Expiry Date
Sep 05, 2027
Product Type
Serological Reagents
Respiratory viral panel multiplex nucleic acid assay
Invitro Diagnostics
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