QIAamp DSP DNA FFPE Tissue Kit - Indonesia BPOM Medical Device Registration
QIAamp DSP DNA FFPE Tissue Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20202024058. 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
Jalan Panjang, Perkantoran Kedoya Elok Plaza Blok DB No. 24
Registration Date
Sep 17, 2024
Expiry Date
May 13, 2029
Product Type
Cell and Tissue Culture Products
Somatic Gene Mutation Detection System
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