CARDIOLINE HD+ - Indonesia BPOM Medical Device Registration
CARDIOLINE HD+ is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502515431. The device is manufactured by CARDIOLINE S.P.A from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is INDOPRIMA BIONET.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CARDIOLINE S.P.ACountry of Origin
Italy
Authorized Representative
INDOPRIMA BIONETAR Address
Jalan Tamansari Raya, Komplek 56 No. 56 B Jakarta Barat 11150
Registration Date
Feb 06, 2023
Expiry Date
Sep 21, 2027
Product Type
Monitoring Cardiology Equipment
Electrocardiograph.
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