AMA Rapid Urease Test Expert - Indonesia BPOM Medical Device Registration
AMA Rapid Urease Test Expert is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303813994. The device is manufactured by ASSOCIATION OF MEDICINE AND ANALYTICS COMPANY, LTD. from Russian Federation, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDQUEST JAYA GLOBAL.
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
Country of Origin
Russian Federation
Authorized Representative
PT. MEDQUEST JAYA GLOBALAR Address
Menara Salemba Lantai 6 Jl. Salemba Raya Kav. 5 - 5A
Registration Date
Aug 04, 2022
Expiry Date
Jul 05, 2027
Product Type
Serological Reagents
Campylobacter fetus serological reagents.
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