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MEDIAN Defibrillator/Monitor - Indonesia BPOM Medical Device Registration

MEDIAN Defibrillator/Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505413099. The device is manufactured by MEDIAN CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. DEMKA SAKTI.

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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Risk Class Kelas Resiko : D
MEDIAN Defibrillator/Monitor

MEDIANA Defibrilator/Monitor

Analysis ID: AKL 30505413099

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

MEDIAN CO., LTD.

Country of Origin

Korea

Authorized Representative

PT. DEMKA SAKTI

AR Address

Jl. Tanah Abang III No. 19 A - B, Jakarta Pusat

Registration Date

Sep 13, 2022

Expiry Date

Jul 31, 2025

Product Type

Therapeutic Cardiology Equipment

Automated external defibrillator.

Non Radiation Electromedics

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