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IGEL Patient Monitor - Indonesia BPOM Medical Device Registration

IGEL Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502121719. The device is manufactured by PROFESSIONAL ELECTRONICS COMPANY IGEL from Poland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GAMAMED.

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BPOM Registered
Risk Class Kelas Resiko : B
IGEL Patient Monitor
Analysis ID: AKL 20502121719

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Poland

Authorized Representative

PT. GAMAMED

AR Address

JL. WR. SUPRATMAN 56 B

Registration Date

Mar 30, 2021

Expiry Date

Dec 20, 2025

Product Type

Monitoring Cardiology Equipment

Cardiac monitor (including cardiotachometer and rate alarm).

Non Radiation Electromedics

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