Pure Global

MEDIANA Body Composition Analyzer I50 - Indonesia BPOM Medical Device Registration

MEDIANA Body Composition Analyzer I50 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502320825. The device is manufactured by MEDIAN CO.,LTD from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ASA PRATAMA PARTNERS.

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
MEDIANA Body Composition Analyzer I50
Analysis ID: AKL 20502320825

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

MEDIAN CO.,LTD

Country of Origin

Korea

Authorized Representative

PT. ASA PRATAMA PARTNERS

AR Address

MT Haryono Square No.OF 01/06 JL. MT.Haryono Kav.10, Kel. Bidara Cina , Kec. Jatinegara - Jakarta Timur

Registration Date

Sep 20, 2023

Expiry Date

Jun 07, 2026

Product Type

Monitoring Cardiology Equipment

Impedance plethysmograph.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing