VIDAMED Patient Monitor - Indonesia BPOM Medical Device Registration
VIDAMED Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502220151. The device is manufactured by SHENZHEN COMEN MEDICAL INSTRUMENT CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ARIMIA JAYA MANDIRI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHENZHEN COMEN MEDICAL INSTRUMENT CO., LTDCountry of Origin
China
Authorized Representative
ARIMIA JAYA MANDIRIAR Address
Jl. Cempaka Putih Timur XXIV No. 78A Belakang BCA KCP Cempaka Putih
Registration Date
Feb 01, 2025
Expiry Date
Jan 31, 2028
Product Type
Monitoring Cardiology Equipment
Cardiac monitor (including cardiotachometer and rate alarm).
Non Radiation Electromedics
