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TRIONARA Central Monitoring System - Indonesia BPOM Medical Device Registration

TRIONARA Central Monitoring System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502320717. The device is manufactured by TRIONARA TECHNOLOGIES. from Sweden, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GLOBAL SYSTECH MEDIKA.

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BPOM Registered
Risk Class Kelas Resiko : B
TRIONARA Central Monitoring System
Analysis ID: AKL 20502320717

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Sweden

Authorized Representative

PT. GLOBAL SYSTECH MEDIKA

AR Address

Jl. TB Simatupang No.17 RT.011/002 Kel. Susukan, Kec. Ciracas Jakarta Timur

Registration Date

Jul 06, 2023

Expiry Date

Mar 21, 2026

Product Type

Monitoring Cardiology Equipment

Cardiac monitor (including cardiotachometer and rate alarm).

Non Radiation Electromedics

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