CFX Opus 384 Dx - Indonesia BPOM Medical Device Registration
CFX Opus 384 Dx is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102420363. 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 ANDAMAN MEDICAL INDONESIA.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
BIO-RAD LABORATORIES (SINGAPORE) PTE LTDCountry of Origin
Singapore
Authorized Representative
ANDAMAN MEDICAL INDONESIAAR Address
Menara Cardig Lantai 1, Jalan Raya Halim Perdanakusuma
Registration Date
Nov 01, 2024
Expiry Date
Aug 12, 2029
Product Type
Clinical Laboratory Equipment
Instrumentation for clinical multiplex test systems.
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