QIAstat-Dx Respiratory SARS-CoV-2 Panel - Indonesia BPOM Medical Device Registration
QIAstat-Dx Respiratory SARS-CoV-2 Panel is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303321261. The device is manufactured by QIAGEN GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. UBC MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
QIAGEN GMBH.Country of Origin
Germany
Authorized Representative
PT. UBC MEDICAL INDONESIAAR Address
Jalan Rawa Gelam V, Blok L Kav. 11-13, Kawasan Industri Pulogadung Jakarta Timur13930
Registration Date
Jul 14, 2023
Expiry Date
Nov 08, 2027
Product Type
Serological Reagents
Respiratory viral panel multiplex nucleic acid assay
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