FLEXMAP 3D® System - Indonesia BPOM Medical Device Registration
FLEXMAP 3D® System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102320502. The device is manufactured by LUMINEX CORPORATION from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is GENECRAFT LABS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LUMINEX CORPORATIONCountry of Origin
United States
Authorized Representative
GENECRAFT LABSAR Address
Business Park kebon Jeruk Blok F2 No 9 Jl. Meruya Ilir Raya No. 88
Registration Date
May 10, 2023
Expiry Date
Sep 05, 2027
Product Type
Clinical Laboratory Equipment
Instrumentation for clinical multiplex test systems.
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