EF MEDICA Infant Electrode - Indonesia BPOM Medical Device Registration
EF MEDICA Infant Electrode is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502310348. The device is manufactured by EF MEDICA S.R.L 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
EF MEDICA S.R.LCountry of Origin
Italy
Authorized Representative
PT. INDOPRIMA BIONETAR Address
Jalan Tamansari Raya, Komplek 56 No. 56 B Jakarta Barat 11150
Registration Date
May 29, 2019
Expiry Date
Apr 14, 2024
Product Type
Monitoring Cardiology Equipment
Electrocardiograph electrode.
Non Electromedic Non Sterile
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