Pure Global

FX CorDiax 80 - Indonesia BPOM Medical Device Registration

FX CorDiax 80 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805320675. The device is manufactured by FRESENIUS MEDICAL CARE JAPAN K.K. from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FRESENIUS MEDICAL CARE INDONESIA.

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 : C
FX CorDiax 80
Analysis ID: AKL 20805320675

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. FRESENIUS MEDICAL CARE INDONESIA

AR Address

Tempo Scan Tower Lt.20 JL. HR Rasuna Said Kav 3-4, Kuningan , Jakarta Selatan

Registration Date

Apr 10, 2023

Expiry Date

Feb 04, 2026

Product Type

Therapeutic Gastroenterology-Urology Equipment

Hemodialysis system and accessories.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from FRESENIUS MEDICAL CARE JAPAN K.K.
Products from the same manufacturer (1 products)