SUZUKEN Kenz ECG 305 - Indonesia BPOM Medical Device Registration
SUZUKEN Kenz ECG 305 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502610625. The device is manufactured by SUZUKEN CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SEKARGUNA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SUZUKEN CO., LTD.Country of Origin
Japan
Authorized Representative
PT. SEKARGUNA MEDIKAAR Address
jl.Ciputat Raya no 14 B.Pondok Pinang
Registration Date
Dec 10, 2022
Expiry Date
Sep 28, 2025
Product Type
Monitoring Cardiology Equipment
Electrocardiograph.
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