EKF Quo-Test A1C - Indonesia BPOM Medical Device Registration
EKF Quo-Test A1C is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207810890. The device is manufactured by QUOTIENT DIAGNOSTICS LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MITRA BAHAGIA CITRA MEDIKA.
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
QUOTIENT DIAGNOSTICS LTD.Country of Origin
United Kingdom
Authorized Representative
MITRA BAHAGIA CITRA MEDIKAAR Address
Jl. Raya Kalirungkut 27 Blok C-63
Registration Date
Dec 26, 2022
Expiry Date
Dec 31, 2026
Product Type
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