TRUESCOPE® Multi Parameter Patient Monitor - Indonesia BPOM Medical Device Registration
TRUESCOPE® Multi Parameter Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502125316. 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 PT. MULYA HUSADA JAYA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GUANGDONG BIOLIGHT MEDITECH CO.,LTD.Country of Origin
China
Authorized Representative
PT. MULYA HUSADA JAYAAR Address
JALAN KERINCI NO 2A
Registration Date
Jul 07, 2022
Expiry Date
Dec 31, 2023
Product Type
Monitoring Cardiology Equipment
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