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AESCULON Non Invasive Cardiac Output Electrical Cardiometry - Indonesia BPOM Medical Device Registration

AESCULON Non Invasive Cardiac Output Electrical Cardiometry is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501212984. The device is manufactured by OSYPKA MEDICAL GMBH. from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is INDOPRIMA BIONET.

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BPOM Registered
Risk Class Kelas Resiko : C
AESCULON Non Invasive Cardiac Output Electrical Cardiometry
Analysis ID: AKL 20501212984

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

INDOPRIMA BIONET

AR Address

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

Registration Date

Mar 06, 2024

Expiry Date

May 01, 2028

Product Type

Diagnostic Cardiology Equipment

Arrhythmia detector and alarm (including ST-segment measurement and alarm).

Non Radiation Electromedics

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