QIAstat-Dx® Analyzer 2.0 - Indonesia BPOM Medical Device Registration
QIAstat-Dx® Analyzer 2.0 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102420366. The device is manufactured by LRE MEDICAL 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
LRE MEDICAL GMBHCountry 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
Nov 01, 2024
Expiry Date
May 13, 2028
Product Type
Clinical Laboratory Equipment
Instrumentation for clinical multiplex test systems.
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