CARDIOLINE ECG100L - Indonesia BPOM Medical Device Registration
CARDIOLINE ECG100L is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502910757. The device is manufactured by CARDIOLINE SPA from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INDOPRIMA BIONET.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CARDIOLINE SPACountry of Origin
Italy
Authorized Representative
PT. INDOPRIMA BIONETAR Address
Jalan Tamansari Raya, Komplek 56 No. 56 B Jakarta Barat 11150
Registration Date
Feb 24, 2023
Expiry Date
Sep 21, 2027
Product Type
Monitoring Cardiology Equipment
Electrocardiograph.
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