ARTUS CMV QS-RGQ Kit - Indonesia BPOM Medical Device Registration
ARTUS CMV QS-RGQ Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303711332. The device is manufactured by QIAGEN GMBH. from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. INODIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
QIAGEN GMBH.Country of Origin
Germany
Authorized Representative
PT. INODIAAR Address
Perkantoran Kedoya Elok Plaza Blok DB no 24, Jalan Panjang, Kebon Jeruk
Registration Date
Sep 24, 2020
Expiry Date
Nov 27, 2024
Product Type
Serological Reagents
Cytomegalovirus serological reagents.
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