QIAreach™ QuantiFERON®-TB Test - Indonesia BPOM Medical Device Registration
QIAreach™ QuantiFERON®-TB Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303220003. The device is manufactured by ELLUME LTD from Australia, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. UBC 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
ELLUME LTDCountry of Origin
Australia
Authorized Representative
PT. UBC MEDICAL INDONESIAAR Address
Jalan Rawa Gelam V, Blok L Kav. 11-13, Kawasan Industri Pulogadung Jakarta Timur13930
Registration Date
Jan 04, 2022
Expiry Date
Nov 17, 2026
Product Type
Serological Reagents
Mycobacterium tuberculosis immunofluorescent reagents.
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