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 20502220188. 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., LTD.Country of Origin
China
Authorized Representative
ARIMIA JAYA MANDIRIAR Address
Gedung Konica lantai 3A Jl. Gunung Sahari Raya nomor 78
Registration Date
Jun 10, 2022
Expiry Date
Dec 31, 2024
Product Type
Monitoring Cardiology Equipment
Cardiac monitor (including cardiotachometer and rate alarm).
Non Radiation Electromedics
