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BIOLIGHT Digital Electrogardiograph - Indonesia BPOM Medical Device Registration

BIOLIGHT Digital Electrogardiograph is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502914809. The device is manufactured by GUANGDONG MEDICAL BIOLIGHT from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MAIN MEDICAL FACILITIES.

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
BIOLIGHT Digital Electrogardiograph
Analysis ID: AKL 20502914809

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. MAIN MEDICAL FACILITIES

AR Address

Jl.Tebet Barat Raya No.3 Jakarta 12810

Registration Date

Jul 29, 2019

Expiry Date

Mar 25, 2024

Product Type

Monitoring Cardiology Equipment

Electrocardiograph.

Non Radiation Electromedics

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