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IRADIMED MRI Patient Monitoring System - Indonesia BPOM Medical Device Registration

IRADIMED MRI Patient Monitoring System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502814800. The device is manufactured by IRADIMED CORPORATION. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INTIMEDIKA PUSPA INDAH.

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BPOM Registered
Risk Class Kelas Resiko : B
IRADIMED MRI Patient Monitoring System
Analysis ID: AKL 20502814800

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. INTIMEDIKA PUSPA INDAH

AR Address

JL Gading Kirana Utara Blok E 10 No 32 Kelapa Gading Barat,Kelapa Gading Jakarta Utara

Registration Date

Mar 19, 2024

Expiry Date

May 27, 2027

Product Type

Monitoring Cardiology Equipment

Cardiac monitor (including cardiotachometer and rate alarm).

Non Radiation Electromedics

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