TRISMED CARDIPIA 800 Electrocardiograph - Indonesia BPOM Medical Device Registration
TRISMED CARDIPIA 800 Electrocardiograph is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502913863. The device is manufactured by TRISMED CO, LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PRIMARY WORKS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TRISMED CO, LTD.Country of Origin
Korea
Authorized Representative
PT. PRIMARY WORKSAR Address
Daan Mogot Arcadia Blok F.1/8A-8B Jl. Daan Mogot Km 21, Kelurahan Batu Ceper
Registration Date
Jan 25, 2023
Expiry Date
Dec 21, 2027
Product Type
Monitoring Cardiology Equipment
Electrocardiograph.
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