QIAamp® DSP DNA Blood Mini Kit (50), Version 2 - Indonesia BPOM Medical Device Registration
QIAamp® DSP DNA Blood Mini Kit (50), Version 2 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204122933. The device is manufactured by QIAGEN GMBH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. INODIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
QIAGEN GMBHCountry of Origin
Germany
Authorized Representative
PT. INODIAAR Address
Jalan Panjang, Perkantoran Kedoya Elok Plaza Blok DB No. 24
Registration Date
Sep 06, 2024
Expiry Date
May 13, 2029
Product Type
Reagents and Specimen Providers
General purpose reagent.
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