CARDIOLIFE Automated External Defibrillator AED-2152K - Indonesia BPOM Medical Device Registration
CARDIOLIFE Automated External Defibrillator AED-2152K is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505025523. The device is manufactured by NIHON KOHDEN TOMIOKA CORPORATION TOMIOKA PRODUCTION CENTER. from Japan, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. INDOMEDIK NIAGA PERKASA.
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Risk Classification
Product Class
Kelas : 3
Country of Origin
Japan
Authorized Representative
PT. INDOMEDIK NIAGA PERKASAAR Address
Jl. Raya Kebayoran Lama No.35 RT.008 RW.001 Kelurahan Sukabumi Selatan, Kecamatan Kebon Jeruk, Jakarta Barat, DKI Jakarta
Registration Date
Mar 23, 2023
Expiry Date
Mar 31, 2026
Product Type
Therapeutic Cardiology Equipment
Automated external defibrillator.
Non Radiation Electromedics
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