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ARNEZ Maternal & Fetal Monitor - Indonesia BPOM Medical Device Registration

ARNEZ Maternal & Fetal Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21101320118. 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. SEKARGUNA MEDIKA.

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
ARNEZ Maternal & Fetal Monitor
Analysis ID: AKL 21101320118

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. SEKARGUNA MEDIKA

AR Address

JL. Ciputat Raya Nomor 64

Registration Date

Dec 30, 2023

Expiry Date

May 17, 2026

Product Type

Obstetric and Gynecological Monitoring Equipment

Fetal cardiac monitor.

Non Radiation Electromedics

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