TRUSCOPE III Multi Parameter Patient Monitor - Indonesia BPOM Medical Device Registration
TRUSCOPE III Multi Parameter Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502121288. The device is manufactured by GUANGDONG BIOLIGHT MEDITECH, CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MULYA HUSADA JAYA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GUANGDONG BIOLIGHT MEDITECH, CO.,LTDCountry of Origin
China
Authorized Representative
MULYA HUSADA JAYAAR Address
JALAN KERINCI NO. 2-A
Registration Date
Oct 10, 2023
Expiry Date
Oct 31, 2025
Product Type
Monitoring Cardiology Equipment
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