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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 20502420159. The device is manufactured by Infunix Technolorry 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 20502420159

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

TRIGELS INDONESIA

AR Address

TRIGELS INDONESIA

Registration Date

Apr 30, 2024

Expiry Date

Jul 25, 2028

Product Type

Monitoring Cardiology Equipment

Cardiac monitor (including cardiotachometer and rate alarm).

Non Radiation Electromedics

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