Pure Global

DIALIFE AV Hemodialysis Tubing Set - Indonesia BPOM Medical Device Registration

DIALIFE AV Hemodialysis Tubing Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805220451. The device is manufactured by BAIN MEDICAL EQUIPMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GRAHA KREASI 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
DIALIFE AV Hemodialysis Tubing Set
Analysis ID: AKL 20805220451

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. GRAHA KREASI MEDIKA

AR Address

Pakuwon Tower Kota Kasablanka Lt. 10 Unit J, Jl.Casablanca No. 88

Registration Date

Nov 25, 2022

Expiry Date

Oct 31, 2026

Product Type

Therapeutic Gastroenterology-Urology Equipment

Hemodialysis system and accessories.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing