DIAGCORE Analytical Module - Indonesia BPOM Medical Device Registration
DIAGCORE Analytical Module is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102024848. 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. INODIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LRE MEDICAL GMBH.Country of Origin
Germany
Authorized Representative
PT. INODIAAR Address
Perkantoran Kedoya Elok Plaza Blok DB no 24, Jalan Panjang, Kebon Jeruk
Registration Date
Aug 28, 2020
Expiry Date
Mar 06, 2024
Product Type
Clinical Laboratory Equipment
Instrumentation for clinical multiplex test systems.
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