AXION Defibrillator Monitor - Indonesia BPOM Medical Device Registration
AXION Defibrillator Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505313948. The device is manufactured by AXION JSC. from Russia, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. GLOBAL SYSTECH MEDIKA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
AXION JSC.Country of Origin
Russia
Authorized Representative
PT. GLOBAL SYSTECH MEDIKAAR Address
Jl. TB Simatupang No.17 RT.011/002 Kel. Susukan, Kec. Ciracas Jakarta Timur
Registration Date
Nov 01, 2024
Expiry Date
Sep 28, 2029
Product Type
Therapeutic Cardiology Equipment
Automated external defibrillator.
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