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INFUNIX Patient Monitor - Indonesia BPOM Medical Device Registration

INFUNIX Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502125850. The device is manufactured by INFUNIX TEKHNOLOGY CO,LTD from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is TRIGELS INDONESIA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
INFUNIX Patient Monitor
Analysis ID: AKL 20502125850

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

TRIGELS INDONESIA

AR Address

Ruko Malaka Country Blok A No. 14, Jl. Raya Pondok Kopi RT. 009 RW. 010

Registration Date

Sep 20, 2021

Expiry Date

Dec 17, 2024

Product Type

Monitoring Cardiology Equipment

Cardiac monitor (including cardiotachometer and rate alarm).

Non Radiation Electromedics

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