LIFE SCOPE G7 Bedside Monitor - Indonesia BPOM Medical Device Registration
LIFE SCOPE G7 Bedside Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501023634. The device is manufactured by NIHON KOHDEN TOMIOKA CORPORATION TOMIOKA PRODUCTION CENTER from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. INDOMEDIK NIAGA PERKASA.
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Risk Classification
Product Class
Kelas : 2
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 24, 2023
Expiry Date
Mar 31, 2026
Product Type
Diagnostic Cardiology Equipment
Arrhythmia detector and alarm (including ST-segment measurement and alarm).
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