AIMTECH Patient Monitor - Indonesia BPOM Medical Device Registration
AIMTECH Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502914426. The device is manufactured by SHENZHEN MILLION MEDICAL INSTRUMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ARMICO CORE MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHENZHEN MILLION MEDICAL INSTRUMENT CO., LTD.Country of Origin
China
Authorized Representative
ARMICO CORE MEDIKAAR Address
Jl. Bedugul 1A No. 3
Registration Date
Mar 26, 2022
Expiry Date
Mar 28, 2025
Product Type
Monitoring Cardiology Equipment
Cardiac monitor (including cardiotachometer and rate alarm).
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