Pure Global

BIOLIGHT Digital Electrocardiograph - Indonesia BPOM Medical Device Registration

BIOLIGHT Digital Electrocardiograph is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502125168. 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. KARUNIAJAYA ANDALAN PRIMA.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
BIOLIGHT Digital Electrocardiograph
Analysis ID: AKL 20502125168

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. KARUNIAJAYA ANDALAN PRIMA

AR Address

RUKO JALUR SUTERA TIMUR BLOK. 6B NO. 23 ALAM SUTERA, SERPONG, TANGERANG 15144.

Registration Date

Aug 22, 2021

Expiry Date

Feb 26, 2026

Product Type

Monitoring Cardiology Equipment

Electrocardiograph.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing