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CARDIOLINE Electrocardiograph - Indonesia BPOM Medical Device Registration

CARDIOLINE Electrocardiograph is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502613416. The device is manufactured by CARDIOLINE S.P.A. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INDOPRIMA BIONET.

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BPOM Registered
Risk Class Kelas Resiko : B
CARDIOLINE Electrocardiograph
Analysis ID: AKL 20502613416

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

CARDIOLINE S.P.A.

Country of Origin

Italy

Authorized Representative

PT. INDOPRIMA BIONET

AR Address

Jalan Tamansari Raya, Komplek 56 No. 56 B Jakarta Barat 11150

Registration Date

Feb 24, 2023

Expiry Date

Sep 21, 2027

Product Type

Monitoring Cardiology Equipment

Electrocardiograph.

Non Radiation Electromedics

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