CardiAID Pro Biphasic Defibrillator - Indonesia BPOM Medical Device Registration
CardiAID Pro Biphasic Defibrillator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505718760. The device is manufactured by CARDIA INTERNATIONAL A/S. from Denmark, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MAIN COMMERCIAL HOSPI.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
CARDIA INTERNATIONAL A/S.Country of Origin
Denmark
Authorized Representative
PT. MAIN COMMERCIAL HOSPIAR Address
JALAN LENGKONG KECIL No.66, RT.001/RW.004, KEL. PALEDANG, KEC. LENGKONG, KOTA BANDUNG, Provinsi Jawa Barat, 40261.
Registration Date
Jul 12, 2023
Expiry Date
Sep 13, 2027
Product Type
Therapeutic Cardiology Equipment
Automated external defibrillator.
Non Radiation Electromedics
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