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TRUSCOPE® Modular Patient Monitor - Indonesia BPOM Medical Device Registration

TRUSCOPE® Modular Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502121092. The device is manufactured by GUANGDONG BIOLIGHT MEDITECH, CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MULYA HUSADA JAYA.

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
TRUSCOPE® Modular Patient Monitor
Analysis ID: AKL 20502121092

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. MULYA HUSADA JAYA

AR Address

JALAN KERINCI NO 2A

Registration Date

Jun 22, 2022

Expiry Date

Dec 31, 2023

Product Type

Monitoring Cardiology Equipment

Cardiac monitor (including cardiotachometer and rate alarm).

Non Radiation Electromedics

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