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ARIA High Flux Hemodialyzer - Indonesia BPOM Medical Device Registration

ARIA High Flux Hemodialyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805023993. The device is manufactured by SUZHOU JUNKANG MEDICAL TECHNOLOGY CO. LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. EUROMED CHAKRA MEDICAL.

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 : C
ARIA High Flux Hemodialyzer
Analysis ID: AKL 20805023993

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. EUROMED CHAKRA MEDICAL

AR Address

RUKO MEGA GROSIR CEMPAKA MAS BLOK P.31 JL. LETNAN JENDRAL SUPRAPTO

Registration Date

Jul 17, 2020

Expiry Date

Sep 26, 2024

Product Type

Therapeutic Gastroenterology-Urology Equipment

Hemodialysis system and accessories.

Non Electromedic Sterile

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