AXION Electrocardiograph - Indonesia BPOM Medical Device Registration
AXION Electrocardiograph is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502310789. The device is manufactured by AXION JSC. from Russian Federation, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GLOBAL SYSTECH MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
AXION JSC.Country of Origin
Russian Federation
Authorized Representative
PT. GLOBAL SYSTECH MEDIKAAR Address
Jl. TB Simatupang No.17 RT.011/002 Kel. Susukan, Kec. Ciracas Jakarta Timur
Registration Date
Nov 11, 2019
Expiry Date
Oct 18, 2024
Product Type
Monitoring Cardiology Equipment
Electrocardiograph.
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