ARTUS HI-Virus 1 QS RGQ Kit - Indonesia BPOM Medical Device Registration
ARTUS HI-Virus 1 QS RGQ Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30305615666. The device is manufactured by QIAGEN GMBH from Germany, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. INODIA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
QIAGEN GMBHCountry of Origin
Germany
Authorized Representative
PT. INODIAAR Address
Perkantoran Kedoya Elok Plaza Blok DB no 24, Jalan Panjang, Kebon Jeruk
Registration Date
Sep 28, 2020
Expiry Date
Nov 27, 2024
Product Type
Immunological Test System
Multiple autoantibodies immunological test system.
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