KENZ Digital Holter ECG - Indonesia BPOM Medical Device Registration
KENZ Digital Holter ECG is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502110245. 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 SEKARGUNA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SUZUKEN CO., LTD.Country of Origin
Japan
Authorized Representative
SEKARGUNA MEDIKAAR Address
jl.Ciputat Raya no 14 B.Pondok Pinang
Registration Date
Nov 17, 2020
Expiry Date
Nov 17, 2025
Product Type
Monitoring Cardiology Equipment
Electrocardiograph.
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