CFX Opus 96 Dx with CFX Maestro Dx SE Software - Indonesia BPOM Medical Device Registration
CFX Opus 96 Dx with CFX Maestro Dx SE Software is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102220223. The device is manufactured by BIO-RAD LABORATORIES (SINGAPORE) PTE LTD from Singapore, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ANDAMAN MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BIO-RAD LABORATORIES (SINGAPORE) PTE LTDCountry of Origin
Singapore
Authorized Representative
PT. ANDAMAN MEDICAL INDONESIAAR Address
Menara Cardig Lantai 1, Jalan Raya Halim Perdanakusuma
Registration Date
Sep 10, 2022
Expiry Date
May 04, 2027
Product Type
Clinical Laboratory Equipment
Instrumentation for clinical multiplex test systems.
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