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KENZ CARDICO 601 Electrocardiograph - Indonesia BPOM Medical Device Registration

KENZ CARDICO 601 Electrocardiograph is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502011241. 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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BPOM Registered
Risk Class Kelas Resiko : B
KENZ CARDICO 601 Electrocardiograph
Analysis ID: AKL 20502011241

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

SUZUKEN CO., LTD.

Country of Origin

Japan

Authorized Representative

PT. SEKARGUNA MEDIKA

AR Address

jl.Ciputat Raya no 14 B.Pondok Pinang

Registration Date

Dec 28, 2022

Expiry Date

Sep 28, 2025

Product Type

Monitoring Cardiology Equipment

Electrocardiograph.

Non Radiation Electromedics

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